Canonical Allele Identifier: PA916032210
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407592
ClinVar RCV Id: RCV000465996 RCV002429500 RCV003993967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp831Asn
CA16613093
NM_001351834.2:c.2491G>A