Canonical Allele Identifier: PA916034529
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 220064
ClinVar RCV Id: RCV000204776 RCV000567581 RCV003477687 RCV004547478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr2627Cys
CA348974
NM_001351834.2:c.7880A>G