Canonical Allele Identifier: PA141442
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47587
ClinVar RCV Id: RCV000040856 RCV000266897 RCV000297925 RCV000324467 RCV000354697 RCV000407527 RCV000726291 RCV001088537 RCV002362658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly32581Val
CA141439
NM_001267550.2:c.97742G>T