Canonical Allele Identifier: PA1139728639
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 967977
ClinVar RCV Id: RCV001243013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341508.1:p.Arg224Ser
CA354826060
NM_001354579.2:c.672G>T
CA354826061
NM_001354579.2:c.672G>C