Allele Registry

Canonical Allele Identifier: PA2825031800

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001181686

ClinVar Variation:

921931

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Lys827Thr	CA382543190 NM_000051.4:c.2480A>C