Canonical Allele Identifier: PA645498684
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232087
ClinVar RCV Id: RCV000214351 RCV000698809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile232Ser
CA10578971
NM_000051.4:c.695T>G