Canonical Allele Identifier: PA645503770
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 420728
ClinVar RCV Id: RCV000478252 RCV001026026 RCV001204431
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2364Pro
CA6266068
NM_000051.4:c.7090G>C