Canonical Allele Identifier: PA2828701698
Gene: EGLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1414304
ClinVar RCV Id: RCV001928620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364189.1:p.Met1Ile
CA345239685
NM_001377260.1:c.3G>T
CA345239686
NM_001377260.1:c.3G>A
CA345239689
NM_001377260.1:c.3G>C