Canonical Allele Identifier: PA2826093189
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1363368
ClinVar RCV Id: RCV001902220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Arg481Trp
CA9226435
NM_001173498.2:c.1441C>T