Canonical Allele Identifier: PA2825031946
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 925965
ClinVar RCV Id: RCV001188233 RCV002249771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala886Gly
CA382545048
NM_000051.4:c.2657C>G