Canonical Allele Identifier: PA1139736372
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 843583
ClinVar RCV Id: RCV001046242 RCV002320264
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1103Glu
CA6265261
NM_001351834.2:c.3309T>A
CA382517398
NM_001351834.2:c.3309T>G