Canonical Allele Identifier: PA1139729786
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 922945
ClinVar RCV Id: RCV001183307
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2635Asp
CA6266208
NM_001351834.2:c.7904C>A