Canonical Allele Identifier: PA339941
Gene: PC HGNC NCBI
ClinVar RCV:
RCV000002177
ClinVar Variation:
2096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Val145Ala
CA339940
NM_001040716.2:c.434T>C