Canonical Allele Identifier: PA2825032443
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 843583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1103Glu
CA6265261
NM_000051.4:c.3309T>A
CA382517398
NM_000051.4:c.3309T>G