Canonical Allele Identifier: PA339943
Gene: PC HGNC NCBI
ClinVar RCV:
RCV000002178
ClinVar Variation:
2097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Arg451Cys
CA339942
NM_001040716.2:c.1351C>T