Canonical Allele Identifier: PA111772
Gene: PROC HGNC NCBI
ClinVar RCV:
RCV000000702
ClinVar Variation:
667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000303.1:p.Pro289Leu
CA114408
NM_000312.4:c.866C>T