Canonical Allele Identifier: PA658740610
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490548
ClinVar RCV Id: RCV000582025 RCV003605663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile1271Val
CA382524805
NM_000051.4:c.3811A>G