Canonical Allele Identifier: PA915990415
Gene: CHKB HGNC NCBI

Linked Data

ClinVar Variation Id: 646146
ClinVar RCV Id: RCV000800374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005189.2:p.Tyr72His
CA10323884
NM_005198.5:c.214T>C