Canonical Allele Identifier: PA916034521
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827299
ClinVar RCV Id: RCV001026893 RCV003467694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys2624Gly
CA382561410
NM_001351834.2:c.7870T>G