Canonical Allele Identifier: PA1139738841
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 919070
ClinVar RCV Id: RCV001176996 RCV003605733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn1860Ser
CA382546125
NM_001351834.2:c.5579A>G