Canonical Allele Identifier: PA2580113867
Gene: NEU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416340
ClinVar RCV Id: RCV003107089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000425.1:p.Ser144Asn
CA363494787
NM_000434.4:c.431G>A