Canonical Allele Identifier: PA2825035681
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2130896
ClinVar RCV Id: RCV003052316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2556Ser
CA382560963
NM_000051.4:c.7666A>T
CA382560965
NM_000051.4:c.7667C>G