Canonical Allele Identifier: PA645503836
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236773
ClinVar RCV Id: RCV000228986 RCV001026398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr2470Cys
CA10582852
NM_000051.4:c.7409A>G