Canonical Allele Identifier: PA2580127652
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2420131
ClinVar RCV Id: RCV003118656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Ala417Val
CA404247497
NM_000528.4:c.1250C>T