Allele Registry

Canonical Allele Identifier: PA2825031177

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001804402

ClinVar Variation:

1331886

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Leu546Met	CA382534523 NM_000051.4:c.1636C>A