Canonical Allele Identifier: PA915994394
Gene: PCCB HGNC NCBI
ClinVar Allele:
47483
ClinVar RCV:
RCV000032129
ClinVar Variation:
38880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Leu539Pro
CA343141
NM_001178014.2:c.1616T>C