Canonical Allele Identifier: PA2573185094
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 1482086
ClinVar RCV Id: RCV001994414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Glu191Asp
CA354739920
NM_001178014.2:c.573G>C
CA354739921
NM_001178014.2:c.573G>T