Canonical Allele Identifier: PA2830209233
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val32635Ala
CA1985231
NM_133378.4:c.97904T>C