Canonical Allele Identifier: PA658743649
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 489570
ClinVar RCV Id: RCV000579988 RCV002529084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr2129His
CA382553307
NM_000051.4:c.6385T>C