Canonical Allele Identifier: PA658669809
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2003Glu
CA382549780
NM_000051.4:c.6009T>G
CA382549782
NM_000051.4:c.6009T>A