Canonical Allele Identifier: PA916035135
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453356
ClinVar RCV Id: RCV000560752 RCV001185975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Val4Ala
CA382518955
NM_001351836.2:c.11T>C