Allele Registry

Canonical Allele Identifier: PA151931

Gene: ATM HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000116427

RCV000131720

RCV000316554

RCV000710673

RCV001194298

RCV001423192

RCV002221615

RCV002225338

RCV002348640

RCV003229020

RCV003315664

ClinVar Variation:

128458

929198

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asp1853Asn	CA151929 NM_000051.4:c.5557G>A CA1139662321 NM_000051.4:c.5556_5557delinsGA