Canonical Allele Identifier: PA916033874
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478959
ClinVar RCV Id: RCV000571659 RCV000797659 RCV003459269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro2093Ser
CA228403260
NM_001351834.2:c.6277C>T