Canonical Allele Identifier: PA103447
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 12015
ClinVar RCV Id: RCV000012795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Glu168Lys
CA341173
NM_000532.5:c.502G>A