Canonical Allele Identifier: PA1139734902
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 924232
ClinVar RCV Id: RCV001185435 RCV001862913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr741Phe
CA382539130
NM_001351834.2:c.2222A>T