Canonical Allele Identifier: PA2827270482
Gene: DPCD HGNC NCBI

Linked Data

ClinVar Variation Id: 91991
ClinVar RCV Id: RCV000122548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316671.1:p.Thr4Met
CA232308
NM_001329742.2:c.11C>T