Canonical Allele Identifier: PA916065381
Gene: PC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071504.2:p.Arg583Leu
CA252102
NM_022172.3:c.1748G>T