Canonical Allele Identifier: PA645453663
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 384218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110440.1:p.Thr706Ala
CA6170972
NM_030813.6:c.2116A>G