Canonical Allele Identifier: PA1139690853
Gene: NEU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 904516
ClinVar RCV Id: RCV001152488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000425.1:p.Val406Glu
CA363484726
NM_000434.4:c.1217T>A