Canonical Allele Identifier: PA1139679931
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 968152
ClinVar RCV Id: RCV001243218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg668His
CA224837120
NM_001127180.2:c.2003G>A