Canonical Allele Identifier: PA242908
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 196099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ser1176Asn
CA242907
NM_000260.4:c.3527G>A