Canonical Allele Identifier: PA645436372
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 328269
ClinVar RCV Id: RCV000343915
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Ala479Ser
CA9226440
NM_000528.4:c.1435G>T