Canonical Allele Identifier: PA114393
Gene: PROC HGNC NCBI
ClinVar RCV:
RCV000000695
ClinVar Variation:
660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000303.1:p.Ala301Val
CA114391
NM_000312.4:c.902C>T