Canonical Allele Identifier: PA298206
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181942
ClinVar RCV Id: RCV000258119 RCV001093019 RCV001175687 RCV003137690 RCV001355020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met1Val