Canonical Allele Identifier: PA132296
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg120Ser
CA132295
NM_000260.4:c.358C>A