Canonical Allele Identifier: PA2825033010
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1059019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn1356Thr
CA382528104
NM_000051.4:c.4067A>C