Canonical Allele Identifier: PA221079
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 93209
ClinVar RCV Id: RCV000079072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Phe408Leu
CA221078
NM_000528.4:c.1224C>A
CA404247734
NM_000528.4:c.1224C>G
CA404247755
NM_000528.4:c.1222T>C