Canonical Allele Identifier: PA335932
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 216193
ClinVar RCV Id: RCV000195774 RCV000221613 RCV000479071 RCV000780905 RCV003474956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val648Ala
CA335930
NM_000051.4:c.1943T>C