Canonical Allele Identifier: PA2825031839
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 924631
ClinVar RCV Id: RCV001186105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr842Ile
CA382543520
NM_000051.4:c.2525C>T