Canonical Allele Identifier: PA2826117469
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1757907
ClinVar RCV Id: RCV002371101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Pro242Ser
CA354825827
NM_001184.4:c.724C>T