Canonical Allele Identifier: PA2828320076
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Val668Ile
CA132233
NM_001369365.1:c.2002G>A