Canonical Allele Identifier: PA916034517
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 449346
ClinVar RCV Id: RCV000521492 RCV001386702 RCV001026887 RCV003319205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2622Val
CA382561402
NM_001351834.2:c.7865C>T