Canonical Allele Identifier: PA2573176369
Gene: PRCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1522543
ClinVar RCV Id: RCV002036085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071088.1:p.Gly32Val
CA8787910
NM_001077620.3:c.95G>T