Canonical Allele Identifier: PA916034545
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 802790
ClinVar RCV Id: RCV000988730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2639Asn
CA382561510
NM_001351834.2:c.7917G>C
CA382561511
NM_001351834.2:c.7917G>T