Canonical Allele Identifier: PA3069370239
Gene: BCHE HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Glu479Asp
CA355110648
NM_000055.4:c.1437A>T
CA355110649
NM_000055.4:c.1437A>C