Canonical Allele Identifier: PA916034634
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141760
ClinVar RCV Id: RCV000130392 RCV001044776
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2708Glu
CA166315
NM_001351834.2:c.8124T>A
CA382562173
NM_001351834.2:c.8124T>G