Canonical Allele Identifier: PA2741809139
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 2620630
ClinVar RCV Id: RCV003384850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Phe365Leu
CA2692374
NM_000055.4:c.1095C>G
CA355111418
NM_000055.4:c.1095C>A
CA355111423
NM_000055.4:c.1093T>C