Canonical Allele Identifier: PA2828621289
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362534.1:p.Ser346Leu
CA114431
NM_001375605.1:c.1037C>T