Canonical Allele Identifier: PA2826117843
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 3221035
ClinVar RCV Id: RCV004507891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Val372Leu
CA354823663
NM_001184.4:c.1114G>T
CA354823664
NM_001184.4:c.1114G>C