Canonical Allele Identifier: PA298036
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181884
ClinVar RCV Id: RCV000159643 RCV000693596 RCV001025519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2224Thr
CA298034
NM_000051.4:c.6671T>C