Canonical Allele Identifier: PA2825036071
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827488
ClinVar Variation Id: 1171554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2725Glu
CA382562503
NM_000051.4:c.8175T>A
CA382562504
NM_000051.4:c.8175T>G