Canonical Allele Identifier: PA166317
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141760
ClinVar RCV Id: RCV000130392 RCV001044776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2708Glu
CA166315
NM_000051.4:c.8124T>A
CA382562173
NM_000051.4:c.8124T>G