Canonical Allele Identifier: PA298280
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181968
ClinVar RCV Id: RCV000159735 RCV000567744 RCV000472045 RCV001357645 RCV003338433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe1877Ser
CA298278
NM_000051.4:c.5630T>C