Canonical Allele Identifier: PA2573186342
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1365271
ClinVar RCV Id: RCV001929749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Ala341Val
CA9226638
NM_001173498.2:c.1022C>T