Canonical Allele Identifier: PA132446
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gly2214Ser
CA132445
NM_000260.4:c.6640G>A