Canonical Allele Identifier: PA645426806
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gln188Glu
CA6197170
NM_000260.4:c.562C>G