Canonical Allele Identifier: PA658826516
Gene: BCHE HGNC NCBI
ClinVar RCV:
RCV000664821
ClinVar Variation:
550155
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Arg498Trp
CA2692299
NM_000055.4:c.1492C>T