Canonical Allele Identifier: PA181827
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178221
ClinVar RCV Id: RCV000157561 RCV000154956 RCV000243216 RCV000852863 RCV001080889 RCV000724471 RCV001131898 RCV001798509 RCV001131899 RCV001132870 RCV001132871 RCV001132872 RCV004544426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro10722Thr
CA181826
NM_133378.4:c.32164C>A