Canonical Allele Identifier: PA096771
Gene: PRCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1400851
ClinVar RCV Id: RCV001896782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071088.1:p.Val30Met
CA8787909
NM_001077620.3:c.88G>A