Canonical Allele Identifier: PA2825035822
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1059998
ClinVar RCV Id: RCV001369368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2622Thr
CA382561399
NM_000051.4:c.7864G>A