Canonical Allele Identifier: PA2573204708
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1355673
ClinVar RCV Id: RCV001867040 RCV002458660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser865Asn
CA382544053
NM_001351834.2:c.2594G>A