Canonical Allele Identifier: PA2828621569
Gene: PROC HGNC NCBI
ClinVar RCV:
RCV000000695
ClinVar Variation:
660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362535.1:p.Ala357Val
CA114391
NM_001375606.1:c.1070C>T