Canonical Allele Identifier: PA093217
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 225302
ClinVar RCV Id: RCV000490369 RCV002282044
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Lys295Arg
CA2692410
NM_000055.4:c.884A>G