Canonical Allele Identifier: PA916031269
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478939
ClinVar RCV Id: RCV001348023 RCV000575108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn133Ser
CA382524935
NM_001351834.2:c.398A>G