Canonical Allele Identifier: PA2825035963
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2747011
ClinVar RCV Id: RCV003501947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2688Pro
CA382561969
NM_000051.4:c.8062G>C