Canonical Allele Identifier: PA916033491
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 424994
ClinVar RCV Id: RCV000488329 RCV000698483 RCV002350081 RCV004551597
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys1811Ser
CA16621628
NM_001351834.2:c.5432G>C
CA382544010
NM_001351834.2:c.5431T>A