Canonical Allele Identifier: PA2580158057
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717060
ClinVar RCV Id: RCV002296242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Gly76Asp
CA404258111
NM_001173498.2:c.227G>A