Canonical Allele Identifier: PA915955729
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 729090
ClinVar RCV Id: RCV000903685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Thr6Ser
CA2692580
NM_000055.4:c.16A>T