Allele Registry

Canonical Allele Identifier: PA298237

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000159720

RCV000573270

RCV000703729

RCV001357834

ClinVar Variation:

181953

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Met1321Val	CA298235 NM_000051.4:c.3961A>G