Canonical Allele Identifier: PA915994349
Gene: PCCB HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Tyr459Cys
CA2632149
NM_001178014.2:c.1376A>G