Canonical Allele Identifier: PA111777
Gene: PC HGNC NCBI
ClinVar Allele:
17136
ClinVar RCV:
RCV000002178
ClinVar Variation:
2097
JSON-LD

Amino-acid Alleles

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