Canonical Allele Identifier: PA658804607
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 529437
ClinVar RCV Id: RCV000634872 RCV001193212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Gly162Trp
CA2631758
NM_000532.5:c.484G>T