Canonical Allele Identifier: PA915980888
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 179146
ClinVar RCV Id: RCV001347350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Cys635Arg
CA183808
NM_001127180.2:c.1903T>C