Canonical Allele Identifier: PA916031979
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524398
ClinVar RCV Id: RCV000628160 RCV002413784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser644Thr
CA382536532
NM_001351834.2:c.1930T>A