Canonical Allele Identifier: PA352095
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 222737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Ala151Thr
CA352093
NM_000258.3:c.451G>A