Canonical Allele Identifier: PA645501113
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 418904
ClinVar Variation Id: 453421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp851Glu
CA16619142
NM_000051.4:c.2553T>G
CA382543740
NM_000051.4:c.2553T>A