Canonical Allele Identifier: PA916032913
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 630066
ClinVar RCV Id: RCV000793212 RCV000774982 RCV003322820 RCV003465697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe1336Leu
CA382527507
NM_001351834.2:c.4006T>C
CA382527523
NM_001351834.2:c.4008C>A
CA382527531
NM_001351834.2:c.4008C>G