Canonical Allele Identifier: PA141754
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47709
ClinVar RCV Id: RCV000040978 RCV000172601 RCV000269028 RCV000357546 RCV000328741 RCV000363681 RCV000400183 RCV000621595 RCV001082037 RCV004537123
ClinVar Variation Id: 915801
ClinVar RCV Id: RCV002418602 RCV001171219 RCV002483932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu32959Val
CA141752
NM_133378.4:c.98876A>T
CA60950864
NM_133378.4:c.98874_98876delinsAGT