Canonical Allele Identifier: PA645498955
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly330Glu
CA16613258
NM_000051.4:c.989G>A