Canonical Allele Identifier: PA2580152022
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1794352
ClinVar RCV Id: RCV002428693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Val885Leu
CA354814881
NM_001184.4:c.2653G>T
CA354814884
NM_001184.4:c.2653G>C