Canonical Allele Identifier: PA915980942
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg686His
CA6197677
NM_001127180.2:c.2057G>A