Canonical Allele Identifier: PA2828319613
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Ala288Thr
CA6197298
NM_001369365.1:c.862G>A