Canonical Allele Identifier: PA658655455
Gene: HYDIN HGNC NCBI

Linked Data

ClinVar Variation Id: 445775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257903.1:p.Arg4953Trp
CA8148356
NM_001270974.2:c.14857C>T