ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA298298
Gene: ATM
HGNC
NCBI
Linked Data
ClinVar Variation Id:
181974
ClinVar RCV Id:
RCV000159742
RCV000167946
RCV000212037
RCV000709711
RCV000762824
RCV001391204
RCV001706063
RCV001657897
RCV003162671
RCV004551374
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000042.3:p.Arg2032Lys
CA298296
NM_000051.4:c.6095G>A