Canonical Allele Identifier: PA138699
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46594
ClinVar RCV Id: RCV000039864 RCV000172700 RCV000245398 RCV001083213 RCV000769085 RCV001131803 RCV001131799 RCV001131800 RCV001131801 RCV001131802 RCV004534850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr3713Ser
CA138697
NM_133378.4:c.11138C>G
CA60981745
NM_133378.4:c.11137A>T