Canonical Allele Identifier: PA2580104328
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 2407567
ClinVar RCV Id: RCV002778981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Asp419Val
CA87410314
NM_000055.4:c.1256A>T