Canonical Allele Identifier: PA2499251128
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1024203
ClinVar RCV Id: RCV001324359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1105Tyr
CA382517440
NM_001351834.2:c.3314C>A