Canonical Allele Identifier: PA2825220850
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 451495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Thr1003Met
CA6130922
NM_000920.4:c.3008C>T