Canonical Allele Identifier: PA658673586
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482717
ClinVar RCV Id: RCV000573165 RCV001062842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys331Glu
CA382531245
NM_000051.4:c.991A>G