Canonical Allele Identifier: PA165589
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141486
ClinVar RCV Id: RCV000130040 RCV000543134 RCV000589125 RCV001255215 RCV002478391 RCV003467129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr1350Met
CA165587
NM_000051.4:c.4049C>T