Canonical Allele Identifier: PA2828319698
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 178478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Ile365Val
CA182408
NM_001369365.1:c.1093A>G