Canonical Allele Identifier: PA2825035834
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 802788
ClinVar RCV Id: RCV000988728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2625Glu
CA382561421
NM_000051.4:c.7875T>A
CA382561422
NM_000051.4:c.7875T>G