Canonical Allele Identifier: PA916031516
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 229794
ClinVar RCV Id: RCV000220769 RCV000255507 RCV000526404 RCV001658022 RCV003468983 RCV003165551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro292Leu
CA6264689
NM_001351834.2:c.875C>T