Canonical Allele Identifier: PA137064
Gene: MYO3A HGNC NCBI

Linked Data

ClinVar Variation Id: 45800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059129.3:p.Asp57Ala
CA137063
NM_017433.5:c.170A>C