Canonical Allele Identifier: PA915980754
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 29926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg395His
CA128772
NM_001127180.2:c.1184G>A