Canonical Allele Identifier: PA2580127885
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2144057
ClinVar RCV Id: RCV003053238 RCV003062869
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Gln699His
CA9226200
NM_000528.4:c.2097G>C
CA404243411
NM_000528.4:c.2097G>T