Canonical Allele Identifier: PA2825034265
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1749666
ClinVar RCV Id: RCV002359774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1930Glu
CA382548328
NM_000051.4:c.5790T>A
CA382548329
NM_000051.4:c.5790T>G