Canonical Allele Identifier: PA1139729791
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 926428
ClinVar RCV Id: RCV001189023 RCV002252325 RCV002249772 RCV003500669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2636Ile
CA382561490
NM_001351834.2:c.7907C>T