Canonical Allele Identifier: PA2827629226
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3222670
ClinVar RCV Id: RCV004516054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2317Gln
CA382557309
NM_001351834.2:c.6949A>C