Canonical Allele Identifier: PA2828620660
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362532.1:p.Arg275Trp
CA114410
NM_001375603.1:c.823C>T