Canonical Allele Identifier: PA286830
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127381
ClinVar RCV Id: RCV000115186 RCV000574275 RCV000628153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr1363Ala
CA286828
NM_000051.4:c.4087A>G