Canonical Allele Identifier: PA916032355
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453431
ClinVar RCV Id: RCV000538623 RCV000567965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr910Ala
CA382545340
NM_001351834.2:c.2728A>G