Canonical Allele Identifier: PA2741809141
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 2545443
ClinVar RCV Id: RCV003242639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Asn369Lys
CA355111387
NM_000055.4:c.1107C>G
CA355111388
NM_000055.4:c.1107C>A