Canonical Allele Identifier: PA2825187418
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 1485889
ClinVar RCV Id: RCV002001071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Asn159Lys
CA2631756
NM_000532.5:c.477T>G
CA354739638
NM_000532.5:c.477T>A