Canonical Allele Identifier: PA916033689
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490633
ClinVar RCV Id: RCV000581541 RCV000819757 RCV003465302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe1977Ser
CA6265807
NM_001351834.2:c.5930T>C