Canonical Allele Identifier: PA2825182041
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2146598
ClinVar RCV Id: RCV003067214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Ala250Thr
CA9226727
NM_000528.4:c.748G>A