Canonical Allele Identifier: PA2580127935
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1978956
ClinVar RCV Id: RCV002775186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Ser715Leu
CA305462926
NM_000528.4:c.2144C>T