Canonical Allele Identifier: PA2580206895
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1763203
ClinVar RCV Id: RCV002434863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe2799Leu
CA382516658
NM_001351834.2:c.8395T>C
CA382516674
NM_001351834.2:c.8397T>A
CA382516680
NM_001351834.2:c.8397T>G