Canonical Allele Identifier: PA101317
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208284
ClinVar RCV Id: RCV000206950
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Trp714Arg
CA350952
NM_000528.4:c.2140T>C
CA404243199
NM_000528.4:c.2140T>A