Canonical Allele Identifier: PA2828354721
Gene: PCGF2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356544.1:p.Thr237Asn
CA398820160
NM_001369615.1:c.710C>A