Canonical Allele Identifier: PA107670
Gene: NEU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2456
ClinVar RCV Id: RCV000002560
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000425.1:p.Arg225Pro
CA212564
NM_000434.4:c.674G>C