Canonical Allele Identifier: PA298196
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181938
ClinVar RCV Id: RCV000159705 RCV000234598 RCV001180649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr1029Ser
CA298194
NM_000051.4:c.3085A>T