Canonical Allele Identifier: PA916033736
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481351
ClinVar RCV Id: RCV000575628 RCV001044481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2007Asp
CA382549838
NM_001351834.2:c.6021A>C
CA382549840
NM_001351834.2:c.6021A>T