Canonical Allele Identifier: PA130955
Gene: RTEL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 42021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116575.3:p.Arg981Trp
CA130954
NM_032957.5:c.2941C>T