Canonical Allele Identifier: PA2826679097
Gene: RTEL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269938.1:p.Asn239Ser
CA9964419
NM_001283009.2:c.716A>G