Canonical Allele Identifier: PA2826093194
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1515981
ClinVar RCV Id: RCV002023605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Gly484Ala
CA404246409
NM_001173498.2:c.1451G>C