Canonical Allele Identifier: PA099556
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 177722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gly25Arg
CA278727
NM_000260.4:c.73G>A
CA381926285
NM_000260.4:c.73G>C