Canonical Allele Identifier: PA2826117165
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1737192
ClinVar RCV Id: RCV002359551 RCV003775800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Phe134Leu
CA84756083
NM_001184.4:c.402T>A
CA354827123
NM_001184.4:c.402T>G
CA354827134
NM_001184.4:c.400T>C