Canonical Allele Identifier: PA103438
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 38881
ClinVar RCV Id: RCV000032130 RCV000790698
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Asn536Asp
CA221097
NM_000532.5:c.1606A>G