Canonical Allele Identifier: PA645499195
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232423
ClinVar RCV Id: RCV000214673 RCV000701301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys387Arg
CA10578996
NM_000051.4:c.1160A>G