Canonical Allele Identifier: PA2825031435
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 642029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp658Asn
CA382536833
NM_000051.4:c.1972G>A