Canonical Allele Identifier: PA2826410226
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly632Asp
CA2005945
NM_001256850.1:c.1895G>A