Canonical Allele Identifier: PA916031682
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127332
ClinVar RCV Id: RCV000119195 RCV000120171 RCV000115136 RCV000590142 RCV001356635 RCV004549538 RCV001798307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val410Ala
CA157210
NM_001351834.2:c.1229T>C