Canonical Allele Identifier: PA2826680969
Gene: RTEL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 217520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269939.1:p.Ser317Ala
CA279525
NM_001283010.1:c.949T>G