Canonical Allele Identifier: PA2828319704
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg367Cys
CA132196
NM_001369365.1:c.1099C>T