Canonical Allele Identifier: PA915994386
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 38879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Arg532Cys
CA343140
NM_001178014.2:c.1594C>T