Canonical Allele Identifier: PA1139690748
Gene: NEU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 972055
ClinVar RCV Id: RCV001247990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000425.1:p.Asn129Ser
CA363495066
NM_000434.4:c.386A>G