Canonical Allele Identifier: PA140981
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47432
ClinVar RCV Id: RCV000040701 RCV000172224 RCV001130623 RCV001130624 RCV001130625 RCV001130627 RCV001084560 RCV001130626 RCV003149660 RCV002345324
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser25520Asn
CA140979
NM_133378.4:c.76559G>A