Canonical Allele Identifier: PA2825031172
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 927032
ClinVar RCV Id: RCV001190037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr543Ser
CA382534509
NM_000051.4:c.1627A>T
CA382534511
NM_000051.4:c.1628C>G