Canonical Allele Identifier: PA177375
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Asp576Asn
CA177374
NM_000260.4:c.1726G>A