Canonical Allele Identifier: PA2827044579
Gene: PCNP HGNC NCBI
ClinVar Allele:
2335455
ClinVar RCV:
RCV004187000
ClinVar Variation:
2347466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307329.1:p.Lys10Asn
CA2520657
NM_001320400.1:c.30G>T
CA2520658
NM_001320400.1:c.30G>C