Canonical Allele Identifier: PA2580206770
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2122353
ClinVar RCV Id: RCV003054006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2713Ser
CA382562224
NM_001351834.2:c.8139A>C
CA382562226
NM_001351834.2:c.8139A>T