Allele Registry

Canonical Allele Identifier: PA298298

Gene: ATM HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000159742

RCV000167946

RCV000212037

RCV000709711

RCV000762824

RCV001391204

RCV001657897

RCV001706063

RCV003162671

RCV004551374

ClinVar Variation:

181974

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Arg2032Lys	CA298296 NM_000051.4:c.6095G>A