Canonical Allele Identifier: PA916033914
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232449
ClinVar RCV Id: RCV000219988 RCV000627902 RCV001818534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser2123Gly
CA10579220
NM_001351834.2:c.6367A>G