Canonical Allele Identifier: PA114401
Gene: PROC HGNC NCBI
ClinVar RCV:
RCV000000698
ClinVar Variation:
663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000303.1:p.Gly343Ser
CA114399
NM_000312.4:c.1027G>A