Canonical Allele Identifier: PA916034641
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 448987
ClinVar RCV Id: RCV000819092 RCV000522072 RCV000567578 RCV003470645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2713Thr
CA382562221
NM_001351834.2:c.8138G>C