Canonical Allele Identifier: PA2825031615
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2698425
ClinVar RCV Id: RCV003501029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu739Asp
CA382539099
NM_000051.4:c.2217A>C
CA382539100
NM_000051.4:c.2217A>T