Canonical Allele Identifier: PA2499251849
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1005222
ClinVar RCV Id: RCV001302058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341508.1:p.Leu274Phe
CA2650722
NM_001354579.2:c.822G>T
CA354825387
NM_001354579.2:c.822G>C