Canonical Allele Identifier: PA2580206648
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2453987
ClinVar RCV Id: RCV003188122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2661Val
CA382561762
NM_001351834.2:c.7982A>T