Canonical Allele Identifier: PA2741866515
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3017044
ClinVar RCV Id: RCV003871163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr878Ile
CA382544343
NM_001351834.2:c.2633C>T