Canonical Allele Identifier: PA916034810
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 418777
ClinVar RCV Id: RCV000480686 RCV000566971 RCV000792087 RCV002307513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro2829Leu
CA16619259
NM_001351834.2:c.8486C>T