Canonical Allele Identifier: PA913195494
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 597127
ClinVar RCV Id: RCV000733155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Val119Leu
CA404256576
NM_000528.4:c.355G>T
CA404256577
NM_000528.4:c.355G>C