Canonical Allele Identifier: PA111777
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 2097
ClinVar RCV Id: RCV000002178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Arg451Cys
CA339942
NM_000920.4:c.1351C>T