Canonical Allele Identifier: PA2580127688
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1947611
ClinVar RCV Id: RCV002663456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Thr491Ile
CA404246336
NM_000528.4:c.1472C>T