Canonical Allele Identifier: PA658670265
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482697
ClinVar RCV Id: RCV000574601 RCV000691287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu2422Lys
CA382559752
NM_000051.4:c.7264G>A