Canonical Allele Identifier: PA891845099
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 569124
ClinVar RCV Id: RCV000689672 RCV002343450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser1263Gly
CA382524568
NM_000051.4:c.3787A>G