Canonical Allele Identifier: PA195910
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186801
ClinVar RCV Id: RCV000166452 RCV000235690 RCV001071389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn567Ser
CA195908
NM_000051.4:c.1700A>G