Canonical Allele Identifier: PA198529
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 187785
ClinVar RCV Id: RCV000167542 RCV000487136 RCV002492676 RCV002516522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110440.1:p.Arg408Gly
CA198528
NM_030813.6:c.1222A>G