Canonical Allele Identifier: PA100235
Gene: RTEL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65413
ClinVar RCV Id: RCV000055635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057518.1:p.Ile699Met
CA144779
NM_016434.4:c.2097C>G