Canonical Allele Identifier: PA1139730365
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 853689
ClinVar RCV Id: RCV001058550 RCV001760010 RCV002429677 RCV003467793
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2751Ser
CA382562669
NM_001351834.2:c.8251A>T
CA382562672
NM_001351834.2:c.8252C>G