Canonical Allele Identifier: PA916031576
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127328
ClinVar RCV Id: RCV000115131 RCV000204640 RCV000211955 RCV001174655 RCV001257472 RCV001354564 RCV003492451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg337His
CA286705
NM_001351834.2:c.1010G>A