Canonical Allele Identifier: PA916033911
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453624
ClinVar Variation Id: 2570808
ClinVar RCV Id: RCV003312209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val2119Leu
CA382553165
NM_001351834.2:c.6355G>C
CA382553167
NM_001351834.2:c.6355G>T