Canonical Allele Identifier: PA157085
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 133610
ClinVar RCV Id: RCV000120126 RCV000128879 RCV000204457 RCV000224090 RCV001354699 RCV002221489 RCV002225358 RCV002498555 RCV003149820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro872Ser
CA157083
NM_000051.4:c.2614C>T