Canonical Allele Identifier: PA2827723264
Gene: ENO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2237618
ClinVar RCV Id: RCV004098613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340275.1:p.Asn427Ser
CA17669324
NM_001353346.3:c.1280A>G