Canonical Allele Identifier: PA354808
Gene: CHKB HGNC NCBI

Linked Data

ClinVar Variation Id: 218667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005189.2:p.Pro73Ser
CA249395
NM_005198.5:c.217C>T