Canonical Allele Identifier: PA2580104299
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 2277992
ClinVar RCV Id: RCV002818348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Cys20Gly
CA355113634
NM_000055.4:c.58T>G