Canonical Allele Identifier: PA916034550
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 215980
ClinVar RCV Id: RCV000197870 RCV000215938 RCV000420030 RCV001250432
ClinVar Variation Id: 1929577
ClinVar RCV Id: RCV002635439 RCV003308193 RCV003482417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2642Ser
CA337507
NM_001351834.2:c.7926A>C
CA382561528
NM_001351834.2:c.7926A>T