Canonical Allele Identifier: PA658673584
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482661
ClinVar RCV Id: RCV000561901 RCV001238128 RCV002281114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly330Ala
CA6264715
NM_000051.4:c.989G>C