Canonical Allele Identifier: PA2825034061
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 998937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr1835Ala
CA228389655
NM_000051.4:c.5503A>G