Canonical Allele Identifier: PA107858
Gene: NEU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453
ClinVar RCV Id: RCV000002557
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000425.1:p.Trp240Arg
CA212563
NM_000434.4:c.718T>C
CA363492244
NM_000434.4:c.718T>A