Canonical Allele Identifier: PA111818
Gene: PROC HGNC NCBI
ClinVar RCV:
RCV000000691
ClinVar Variation:
657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000303.1:p.Trp444Cys
CA114387
NM_000312.4:c.1332G>C
CA348406687
NM_000312.4:c.1332G>T