Canonical Allele Identifier: PA658815813
Gene: MYO3A HGNC NCBI

Linked Data

ClinVar Variation Id: 504639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059129.3:p.His142Tyr
CA5444304
NM_017433.5:c.424C>T