Canonical Allele Identifier: PA2825031171
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2774139
ClinVar RCV Id: RCV003585745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr543Ala
CA382534508
NM_000051.4:c.1627A>G