Canonical Allele Identifier: PA916032035
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490451
ClinVar RCV Id: RCV000583287 RCV000792282 RCV001030520 RCV001526953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu686Ile
CA382537468
NM_001351834.2:c.2056C>A