Canonical Allele Identifier: PA294248
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142046
ClinVar RCV Id: RCV000130850 RCV000475427 RCV000515162 RCV000588298 RCV001354773 RCV001731389 RCV003149903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn1081Ser
CA294246
NM_000051.4:c.3242A>G