Canonical Allele Identifier: PA915994241
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 343467
ClinVar RCV Id: RCV000325301 RCV001706552 RCV003950206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Pro219Ser
CA2631791
NM_001178014.2:c.655C>T