Canonical Allele Identifier: PA645504120
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232996
ClinVar RCV Id: RCV000222168 RCV001833226 RCV003469063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2625Ala
CA10579272
NM_000051.4:c.7874A>C