Canonical Allele Identifier: PA916034528
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 489591
ClinVar RCV Id: RCV000579395 RCV001213875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2626Val
CA382561427
NM_001351834.2:c.7877C>T