Canonical Allele Identifier: PA171385
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 158006
ClinVar RCV Id: RCV000145334 RCV000361827 RCV001517033 RCV003126539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Val316Ile
CA171384
NM_001184.4:c.946G>A