Canonical Allele Identifier: PA2825115676
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 813194
ClinVar RCV Id: RCV001199712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg666Pro
CA381939272
NM_000260.4:c.1997G>C