Canonical Allele Identifier: PA296980
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 181439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Arg63Pro
CA013628
NM_000258.3:c.188G>C