Canonical Allele Identifier: PA2573171103
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_000519.2:p.Gly485Ala
CA404246409
NM_000528.4:c.1454G>C