Canonical Allele Identifier: PA2826420982
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala21374Val
CA1990999
NM_001256850.1:c.64121C>T