Canonical Allele Identifier: PA1139732429
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 964354
ClinVar RCV Id: RCV001238559 RCV001526207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His231Leu
CA382529081
NM_001351834.2:c.692A>T