Canonical Allele Identifier: PA2580202040
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2159690
ClinVar RCV Id: RCV003072952 RCV003161749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr175Cys
CA382527560
NM_001351834.2:c.524A>G