Canonical Allele Identifier: PA915994268
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 343470
ClinVar RCV Id: RCV000321726 RCV002504151 RCV003418067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Pro299Leu
CA2631888
NM_001178014.2:c.896C>T