Canonical Allele Identifier: PA916033753
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 826166
ClinVar RCV Id: RCV001024854 RCV001215524
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2022Asp
CA382550064
NM_001351834.2:c.6065G>A