Canonical Allele Identifier: PA1139671129
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 901555
ClinVar RCV Id: RCV001147516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Thr343Ser
CA2692388
NM_000055.4:c.1027A>T
CA355111559
NM_000055.4:c.1028C>G