Canonical Allele Identifier: PA645487582
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 344091
ClinVar RCV Id: RCV000305441 RCV000942318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Asn443His
CA2692336
NM_000055.4:c.1327A>C