Canonical Allele Identifier: PA2828354769
Gene: PCGF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1902857
ClinVar RCV Id: RCV002583249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356544.1:p.Pro339Leu
CA8524840
NM_001369615.1:c.1016C>T