Canonical Allele Identifier: PA645487559
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 254777
ClinVar RCV Id: RCV000251520 RCV000666412
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Glu283Asp
CA2692418
NM_000055.4:c.849G>C
CA355111945
NM_000055.4:c.849G>T