Canonical Allele Identifier: PA339389
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 216211
ClinVar RCV Id: RCV000200558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln1361His
CA339387
NM_000051.4:c.4083G>T
CA382528338
NM_000051.4:c.4083G>C