Canonical Allele Identifier: PA2827628602
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181957
ClinVar RCV Id: RCV000159724 RCV000229615 RCV000445811 RCV000764933 RCV001175058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln95Lys
CA298245
NM_001351834.2:c.283C>A