Canonical Allele Identifier: PA645498607
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233265
ClinVar RCV Id: RCV000218707 RCV002515708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser207Cys
CA10578967
NM_000051.4:c.620C>G