Canonical Allele Identifier: PA2573171106
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1400389
ClinVar RCV Id: RCV001932706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Thr506Lys
CA305470343
NM_000528.4:c.1517C>A