Canonical Allele Identifier: PA916033518
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 655515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1842Ile
CA382545818
NM_001351834.2:c.5524C>A