Canonical Allele Identifier: PA2825031968
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1172453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu896Phe
CA382545165
NM_000051.4:c.2686C>T