Canonical Allele Identifier: PA2825181868
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2163742
ClinVar RCV Id: RCV003092481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Arg144Cys
CA9226817
NM_000528.4:c.430C>T