Canonical Allele Identifier: PA916034535
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453708
ClinVar RCV Id: RCV000548687 RCV004023656
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2630Val
CA382561448
NM_001351834.2:c.7888T>G