Canonical Allele Identifier: PA658827671
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 556881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg666Gln
CA6197659
NM_000260.4:c.1997G>A