Canonical Allele Identifier: PA915980922
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg668Cys
CA132231
NM_001127180.2:c.2002C>T