Canonical Allele Identifier: PA916033037
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453514
ClinVar RCV Id: RCV000548258 RCV000581990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1441Leu
CA6265435
NM_001351834.2:c.4321A>C
CA382531826
NM_001351834.2:c.4321A>T