Canonical Allele Identifier: PA101248
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1688
ClinVar RCV Id: RCV000001756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Pro356Arg
CA339902
NM_000528.4:c.1067C>G