Canonical Allele Identifier: PA181026
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 177931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Arg63Cys
CA013615
NM_000258.3:c.187C>T