Canonical Allele Identifier: PA2573071131
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1331886
ClinVar RCV Id: RCV001804402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu546Met
CA382534523
NM_001351834.2:c.1636C>A