Canonical Allele Identifier: PA103526
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 38880
ClinVar RCV Id: RCV000032129
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Leu519Pro
CA343141
NM_000532.5:c.1556T>C