Canonical Allele Identifier: PA231742
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Glu134Ala
CA010278
NM_000432.4:c.401A>C