Canonical Allele Identifier: PA658674172
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 485195
ClinVar RCV Id: RCV000561287 RCV000687020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr935Ala
CA228407759
NM_000051.4:c.2803A>G