Canonical Allele Identifier: PA2825035848
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 941254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn2632Lys
CA382561466
NM_000051.4:c.7896C>A
CA382561467
NM_000051.4:c.7896C>G