Canonical Allele Identifier: PA2825035906
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 919744
ClinVar RCV Id: RCV001178060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2662Phe
CA382561769
NM_000051.4:c.7984G>T