Canonical Allele Identifier: PA645503672
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 230391
ClinVar RCV Id: RCV000219813 RCV000449493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr2129Asp
CA10579221
NM_000051.4:c.6385T>G