Allele Registry

Canonical Allele Identifier: PA3063088362

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV005529313

ClinVar Variation:

3990948

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Pro313Ser	CA2692404 NM_000055.4:c.937C>T