Canonical Allele Identifier: PA916032894
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142896
ClinVar RCV Id: RCV000132364 RCV000204555 RCV000237005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1322Ile
CA169707
NM_001351834.2:c.3964C>A