Canonical Allele Identifier: PA645501113
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 418904
ClinVar RCV Id: RCV000483479 RCV000569986 RCV000821523 RCV003470538
ClinVar Variation Id: 453421
ClinVar RCV Id: RCV000558049 RCV002431497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp851Glu
CA16619142
NM_000051.4:c.2553T>G
CA382543740
NM_000051.4:c.2553T>A