Canonical Allele Identifier: PA658826516
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 550155
ClinVar RCV Id: RCV000664821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Arg498Trp
CA2692299
NM_000055.4:c.1492C>T