Canonical Allele Identifier: PA915980585
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg120Ser
CA132295
NM_001127180.2:c.358C>A