Canonical Allele Identifier: PA658670560
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu2621Gln
CA382561392
NM_000051.4:c.7861G>C