Canonical Allele Identifier: PA2825030921
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2003165
ClinVar RCV Id: RCV002833152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser433Tyr
CA382533576
NM_000051.4:c.1298C>A