Canonical Allele Identifier: PA2825030325
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2159690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr175Cys
CA382527560
NM_000051.4:c.524A>G