Allele Registry

Canonical Allele Identifier: PA2825036059

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001341953

RCV003442861

RCV003469572

ClinVar Variation:

1038622

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asp2721Val	CA382562477 NM_000051.4:c.8162A>T