Canonical Allele Identifier: PA2826680668
Gene: RTEL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269939.1:p.Asn16Ser
CA9964419
NM_001283010.1:c.47A>G