Canonical Allele Identifier: PA915955730
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 738189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Ile23Val
CA2692572
NM_000055.4:c.67A>G