Canonical Allele Identifier: PA261201
Gene: HYDIN HGNC NCBI

Linked Data

ClinVar Variation Id: 39698
ClinVar RCV Id: RCV000032900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257903.1:p.Val1329Leu
CA261200
NM_001270974.2:c.3985G>T
CA396632487
NM_001270974.2:c.3985G>C