Canonical Allele Identifier: PA2573204082
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1415704
ClinVar RCV Id: RCV001933211
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser426Arg
CA382533443
NM_001351834.2:c.1276A>C
CA382533461
NM_001351834.2:c.1278T>A
CA382533467
NM_001351834.2:c.1278T>G