Canonical Allele Identifier: PA146750
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 93218
ClinVar RCV Id: RCV000079081 RCV000355741 RCV000675485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Thr312Ile
CA146749
NM_000528.4:c.935C>T