Canonical Allele Identifier: PA107659
Gene: NEU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2457
ClinVar RCV Id: RCV000002561 RCV001314931 RCV003323347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000425.1:p.Ala298Val
CA212565
NM_000434.4:c.893C>T