Canonical Allele Identifier: PA2825035824
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2623Phe
CA382561405
NM_000051.4:c.7867C>T