Canonical Allele Identifier: PA107488
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 14065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Glu22Lys
CA010513
NM_000432.4:c.64G>A