Canonical Allele Identifier: PA2828321819
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2756722
ClinVar RCV Id: RCV003566932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gly2165del
CA6199143
NM_001369365.1:c.6493_6495del