Canonical Allele Identifier: PA658673883
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly670Asp
CA228393595
NM_000051.4:c.2009G>A