Canonical Allele Identifier: PA2825187394
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 2758826
ClinVar RCV Id: RCV003511943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Pro154Leu
CA354739596
NM_000532.5:c.461C>T