Canonical Allele Identifier: PA2828320625
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43210
ClinVar RCV Id: RCV000036114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gln1167Pro
CA278651
NM_001369365.1:c.3500A>C