Canonical Allele Identifier: PA310559
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val25651Ala
CA310557
NM_001267550.2:c.76952T>C