Canonical Allele Identifier: PA2826255884
Gene: ENO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2237618
ClinVar RCV Id: RCV004098613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001188412.1:p.Asn334Ser
CA17669324
NM_001201483.4:c.1001A>G