Canonical Allele Identifier: PA103517
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 203883
ClinVar RCV Id: RCV000186089 RCV000441240 RCV001083724 RCV003917704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Leu17Met
CA312824
NM_000532.5:c.49C>A