Canonical Allele Identifier: PA107783
Gene: NEU1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2447
ClinVar RCV Id: RCV000002551 RCV003555898
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000425.1:p.Leu363Pro
CA212559
NM_000434.4:c.1088T>C