Canonical Allele Identifier: PA093295
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 13218
ClinVar RCV Id: RCV000014112 RCV000779401 RCV001753416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Thr271Met
CA122965
NM_000055.4:c.812C>T