Canonical Allele Identifier: PA167884
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 135767
ClinVar RCV Id: RCV000122871 RCV000131258 RCV000589612 RCV001356310 RCV003467085 RCV004551200 RCV001293417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg2105Ser
CA167882
NM_000051.4:c.6315G>C
CA382552179
NM_000051.4:c.6315G>T