Canonical Allele Identifier: PA2826491510
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly632Asp
CA2005945
NM_001267550.2:c.1895G>A