Canonical Allele Identifier: PA2825035149
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 653540
ClinVar RCV Id: RCV000809328 RCV001025816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2312Pro
CA6266034
NM_000051.4:c.6935T>C