Canonical Allele Identifier: PA2828319982
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 636221
ClinVar RCV Id: RCV000787915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gln602Arg
CA381938324
NM_001369365.1:c.1805A>G