Canonical Allele Identifier: PA122394
Gene: TNNC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003271.1:p.Gly159Asp
CA122392
NM_003280.3:c.476G>A