Canonical Allele Identifier: PA2828320639
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43212
ClinVar RCV Id: RCV000036116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gly1180Asp
CA278654
NM_001369365.1:c.3539G>A