Canonical Allele Identifier: PA170060
Gene: PCNA HGNC NCBI

Linked Data

ClinVar Variation Id: 143043
ClinVar RCV Id: RCV000132551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_872590.1:p.Ser228Ile
CA170059
NM_182649.2:c.683G>T