Canonical Allele Identifier: PA2825033020
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1448889
ClinVar RCV Id: RCV001997279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser1360Arg
CA382528275
NM_000051.4:c.4078A>C
CA382528311
NM_000051.4:c.4080T>A
CA382528312
NM_000051.4:c.4080T>G