Canonical Allele Identifier: PA111785
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 2101
ClinVar RCV Id: RCV000002182
JSON-LD

Amino-acid Alleles

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