Canonical Allele Identifier: PA645434569
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 343477

Amino-acid Alleles

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