Canonical Allele Identifier: PA2826093547
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2076838
ClinVar RCV Id: RCV002979493 RCV003308391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Arg707Trp
CA9226196
NM_001173498.2:c.2119C>T