Canonical Allele Identifier: PA658669973
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482630
ClinVar RCV Id: RCV000574099 RCV001350510
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2110Glu
CA6265904
NM_000051.4:c.6330C>G
CA382552262
NM_000051.4:c.6330C>A