Canonical Allele Identifier: PA916034217
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 487014
ClinVar RCV Id: RCV000570715
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2386Ser
CA382559527
NM_001351834.2:c.7156G>T