Canonical Allele Identifier: PA645503719
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231637
ClinVar RCV Id: RCV003605610 RCV000223495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2252Asn
CA10579233
NM_000051.4:c.6755C>A