Canonical Allele Identifier: PA2825033722
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1434321
ClinVar RCV Id: RCV001984606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile1681Arg
CA382540374
NM_000051.4:c.5042T>G