Canonical Allele Identifier: PA915980896
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 450309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg654Cys
CA6197654
NM_001127180.2:c.1960C>T