Canonical Allele Identifier: PA2825031401
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 820361
ClinVar RCV Id: RCV001013739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu643Pro
CA382536526
NM_000051.4:c.1928T>C