Canonical Allele Identifier: PA891845027
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 567725
ClinVar RCV Id: RCV000687890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn870Lys
CA382544157
NM_000051.4:c.2610C>A
CA382544159
NM_000051.4:c.2610C>G