Canonical Allele Identifier: PA2826117421
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1361944
ClinVar RCV Id: RCV001899931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001175.2:p.Phe222Leu
CA2650737
NM_001184.4:c.664T>C
CA354826081
NM_001184.4:c.666T>G
CA354826083
NM_001184.4:c.666T>A