Canonical Allele Identifier: PA3069712439
Gene: BCHE HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Gly388Arg
CA355111259
NM_000055.4:c.1162G>A
CA355111261
NM_000055.4:c.1162G>C