Canonical Allele Identifier: PA2826420903
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 534990

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala21197Val
CA1991092
NM_001256850.1:c.63590C>T