Canonical Allele Identifier: PA2825032986
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1999729
ClinVar RCV Id: RCV002819812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val1345Ala
CA382527733
NM_000051.4:c.4034T>C