Canonical Allele Identifier: PA916034525
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 802788
ClinVar RCV Id: RCV000988728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2625Glu
CA382561421
NM_001351834.2:c.7875T>A
CA382561422
NM_001351834.2:c.7875T>G