Canonical Allele Identifier: PA2825039261
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 3133364
ClinVar RCV Id: RCV004426257

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Asn187Lys
CA87410352
NM_000055.4:c.561T>A
CA355112552
NM_000055.4:c.561T>G