Canonical Allele Identifier: PA2826417880
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val15710Ala
CA1994068
NM_001256850.1:c.47129T>C