Canonical Allele Identifier: PA2825181749
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 892434
ClinVar RCV Id: RCV001128452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Leu78Pro
CA404258039
NM_000528.4:c.233T>C