Canonical Allele Identifier: PA181712
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130680
ClinVar RCV Id: RCV000118781 RCV000154916 RCV000280942 RCV000260854 RCV000375446 RCV000316126 RCV000385773 RCV001081879 RCV002336260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu24265Lys
CA181709
NM_001256850.1:c.72793G>A