Canonical Allele Identifier: PA658669887
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481083
ClinVar RCV Id: RCV000571760
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2058del
CA658656192
NM_000051.4:c.6172_6174del