Canonical Allele Identifier: PA2573246648
Gene: CHKB HGNC NCBI

Linked Data

ClinVar Variation Id: 1374200
ClinVar RCV Id: RCV001877709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005189.2:p.Val71Ala
CA412202995
NM_005198.5:c.212T>C