Canonical Allele Identifier: PA645427098
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg686His
CA6197677
NM_000260.4:c.2057G>A