Canonical Allele Identifier: PA916035132
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 489566
ClinVar RCV Id: RCV000579727 RCV000821860 RCV001569149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Ser2Asn
CA382518922
NM_001351836.2:c.5G>A