Canonical Allele Identifier: PA645502691
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1333Val
CA6265384
NM_000051.4:c.3998A>T