Canonical Allele Identifier: PA2828319560
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg233Pro
CA121720
NM_001369365.1:c.698G>C