Canonical Allele Identifier: PA310558
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202875
ClinVar RCV Id: RCV000184839 RCV001171263 RCV000458395 RCV003482240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val24010Ala
CA310557
NM_001256850.1:c.72029T>C