Canonical Allele Identifier: PA1139685210
Gene: PRCD HGNC NCBI

Linked Data

ClinVar Variation Id: 950646
ClinVar RCV Id: RCV001222400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071088.1:p.Asp29Asn
CA8787905
NM_001077620.3:c.85G>A