Canonical Allele Identifier: PA2828319686
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Leu355Pro
CA278619
NM_001369365.1:c.1064T>C