Canonical Allele Identifier: PA658673809
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu574Asp
CA382535284
NM_000051.4:c.1722A>C
CA382535285
NM_000051.4:c.1722A>T