Canonical Allele Identifier: PA658743763
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 489572
ClinVar RCV Id: RCV000579530 RCV002476262 RCV003605654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr2144Cys
CA382553553
NM_000051.4:c.6431A>G