Canonical Allele Identifier: PA645427026
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 228279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Pro540His
CA6197533
NM_000260.4:c.1619C>A