Canonical Allele Identifier: PA296978
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 181438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Asp62Asn
CA013607
NM_000258.3:c.184G>A