Canonical Allele Identifier: PA2826117782
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1769050
ClinVar RCV Id: RCV002383267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Leu342Val
CA354823978
NM_001184.4:c.1024C>G