Canonical Allele Identifier: PA2825030113
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 660737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg76Ser
CA382521446
NM_000051.4:c.228A>T
CA382521449
NM_000051.4:c.228A>C