Canonical Allele Identifier: PA1139730470
Gene: CHKB HGNC NCBI

Linked Data

ClinVar Variation Id: 943316
ClinVar RCV Id: RCV001213487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005189.2:p.Val74Leu
CA10323881
NM_005198.5:c.220G>C
CA412202930
NM_005198.5:c.220G>T