Canonical Allele Identifier: PA2826117489
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1759249
ClinVar RCV Id: RCV002393749 RCV003099661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Ser250Arg
CA2650728
NM_001184.4:c.750C>G
CA354825700
NM_001184.4:c.750C>A
CA354825714
NM_001184.4:c.748A>C