Allele Registry

Canonical Allele Identifier: PA645504457

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000216939

RCV000628023

ClinVar Variation:

231276

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asp2721His	CA10579285 NM_000051.4:c.8161G>C