Canonical Allele Identifier: PA1139729906
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 919744
ClinVar RCV Id: RCV001178060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val2662Phe
CA382561769
NM_001351834.2:c.7984G>T