Canonical Allele Identifier: PA107840
Gene: NEU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2452
ClinVar RCV Id: RCV000002556 RCV003555900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000425.1:p.Pro80Leu
CA212562
NM_000434.4:c.239C>T