Allele Registry

Canonical Allele Identifier: PA916031614

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000573582

RCV001858236

ClinVar Variation:

482557

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Leu364Ser	CA382532363 NM_001351834.2:c.1091T>C