Canonical Allele Identifier: PA339937
Gene: PC HGNC NCBI
ClinVar Allele:
17133
ClinVar RCV:
RCV000002175
ClinVar Variation:
2094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Ala610Thr
CA339936
NM_001040716.2:c.1828G>A