Canonical Allele Identifier: PA2826471012
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 1676588
ClinVar RCV Id: RCV002221966 RCV002265063 RCV002468655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245321.1:p.Gly530Arg
CA381726572
NM_001258392.1:c.1588G>C
CA381726574
NM_001258392.1:c.1588G>A