Canonical Allele Identifier: PA099538
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 402267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gly2163Ser
CA6199094
NM_000260.4:c.6487G>A