Canonical Allele Identifier: PA2580104327
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 2219748
ClinVar RCV Id: RCV002678004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Gly381Ala
CA2692365
NM_000055.4:c.1142G>C