Canonical Allele Identifier: PA107810
Gene: NEU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000425.1:p.Phe260Tyr
CA212558
NM_000434.4:c.779T>A