Canonical Allele Identifier: PA2825031876
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 821518
ClinVar RCV Id: RCV001016008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp860Glu
CA382543939
NM_000051.4:c.2580T>A
CA382543941
NM_000051.4:c.2580T>G