Canonical Allele Identifier: PA2825030967
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1410688
ClinVar RCV Id: RCV001916528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg451Gly
CA382533778
NM_000051.4:c.1351C>G