Allele Registry

Canonical Allele Identifier: PA3057587558

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV005314037

ClinVar Variation:

3823439

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Pro320Ala	CA2692402 NM_000055.4:c.958C>G