Canonical Allele Identifier: PA2825034468
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1002477
ClinVar RCV Id: RCV001298909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly2024Trp
CA382550090
NM_000051.4:c.6070G>T