Canonical Allele Identifier: PA2580206947
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1763467
ClinVar RCV Id: RCV002447562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met2821Leu
CA382517944
NM_001351834.2:c.8461A>C
CA382517947
NM_001351834.2:c.8461A>T