Canonical Allele Identifier: PA2828319961
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1511284
ClinVar RCV Id: RCV002016606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gly589Ser
CA381938139
NM_001369365.1:c.1765G>A