Canonical Allele Identifier: PA2573171130
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423612
ClinVar RCV Id: RCV001954855 RCV003167258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Leu685Ser
CA9226208
NM_000528.4:c.2054T>C