Canonical Allele Identifier: PA2825031210
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1338030
ClinVar RCV Id: RCV001822628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu560Val
CA382535150
NM_000051.4:c.1679A>T