Canonical Allele Identifier: PA2825181819
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2109517
ClinVar RCV Id: RCV003038404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Tyr118Asp
CA404256621
NM_000528.4:c.352T>G