Canonical Allele Identifier: PA916031565
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407578
ClinVar RCV Id: RCV000457335 RCV002379443 RCV003470425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly330Glu
CA16613258
NM_001351834.2:c.989G>A