Canonical Allele Identifier: PA658669984
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2122Ser
CA382553209
NM_000051.4:c.6364A>T
CA382553215
NM_000051.4:c.6365C>G