Canonical Allele Identifier: PA658661902
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 451495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Thr1003Met
CA6130922
NM_001040716.2:c.3008C>T