Canonical Allele Identifier: PA2825187472
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 2154348
ClinVar RCV Id: RCV003081740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Tyr176Cys
CA354739967
NM_000532.5:c.527A>G