Canonical Allele Identifier: PA645374347
Gene: HYDIN HGNC NCBI

Linked Data

ClinVar Variation Id: 402955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257903.1:p.Glu2306Gly
CA8150096
NM_001270974.2:c.6917A>G