Canonical Allele Identifier: PA2825181722
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051974
ClinVar RCV Id: RCV001360084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Thr71Ile
CA404258295
NM_000528.4:c.212C>T