Canonical Allele Identifier: PA916034518
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827297
ClinVar RCV Id: RCV001026890 RCV003329366 RCV003467693 RCV003605728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2623Phe
CA382561405
NM_001351834.2:c.7867C>T