Canonical Allele Identifier: PA916033485
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 629859
ClinVar RCV Id: RCV000774650
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1806Leu
CA382543863
NM_001351834.2:c.5416A>C
CA382543867
NM_001351834.2:c.5416A>T