Canonical Allele Identifier: PA658670633
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 479035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2667Leu
CA382561792
NM_000051.4:c.7999A>C
CA382561793
NM_000051.4:c.7999A>T