Canonical Allele Identifier: PA310955
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203005
ClinVar RCV Id: RCV000217908 RCV000468035 RCV000728623 RCV001132940 RCV001132938 RCV001132939 RCV001131992 RCV001132941 RCV004537560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val31518Ala
CA310953
NM_001267550.2:c.94553T>C