Canonical Allele Identifier: PA111785
Gene: PC HGNC NCBI
ClinVar Allele:
17140
ClinVar RCV:
RCV000002182
ClinVar Variation:
2101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Arg583Leu
CA252102
NM_000920.4:c.1748G>T