Canonical Allele Identifier: PA645501631
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 234020
ClinVar RCV Id: RCV000220781 RCV000462986 RCV000757014 RCV003330592 RCV003491988 RCV003469092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg1086Cys
CA6265233
NM_000051.4:c.3256C>T