Canonical Allele Identifier: PA298146
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181920
ClinVar RCV Id: RCV000159685 RCV000196810 RCV000590025 RCV003230420 RCV003462071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile576Thr
CA298144
NM_000051.4:c.1727T>C