Canonical Allele Identifier: PA658661901
Gene: PC HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Val890Phe
CA381492401
NM_001040716.2:c.2668G>T