Canonical Allele Identifier: PA2825114328
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 802700
ClinVar Variation Id: 1916542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gly7Arg
CA6197006
NM_000260.4:c.19G>A
CA381947459
NM_000260.4:c.19G>C