Allele Registry

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Canonical Allele Identifier: PA916031999

Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407501

ClinVar RCV Id: RCV000474729 RCV000564798 RCV003493577

ClinVar Variation Id: 937882

ClinVar RCV Id: RCV001207000

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Lys659Asn	CA16613349 NM_001351834.2:c.1977G>T CA382536859 NM_001351834.2:c.1977G>C