Canonical Allele Identifier: PA645434569
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 343477
ClinVar RCV Id: RCV000392658 RCV000626699 RCV000859703 RCV003957774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Lys474Arg
CA2632188
NM_000532.5:c.1421A>G