Canonical Allele Identifier: PA2828320021
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1693020
ClinVar RCV Id: RCV002259447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Ile625Val
CA381938567
NM_001369365.1:c.1873A>G