Canonical Allele Identifier: PA298101
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181905
ClinVar RCV Id: RCV000159669 RCV000221585 RCV000531722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn3003Ser
CA298099
NM_000051.4:c.9008A>G