Canonical Allele Identifier: PA645485227
Gene: MYO3A HGNC NCBI

Linked Data

ClinVar Variation Id: 299646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059129.3:p.Asp204Asn
CA5444383
NM_017433.5:c.610G>A