Canonical Allele Identifier: PA916032946
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 216211
ClinVar RCV Id: RCV000200558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln1361His
CA339387
NM_001351834.2:c.4083G>T
CA382528338
NM_001351834.2:c.4083G>C