Canonical Allele Identifier: PA2826117161
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1041343
ClinVar RCV Id: RCV001345142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Phe132Leu
CA2650772
NM_001184.4:c.396T>A
CA354827144
NM_001184.4:c.396T>G
CA354827157
NM_001184.4:c.394T>C