Canonical Allele Identifier: PA2825034757
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3222349
ClinVar RCV Id: RCV004513763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2148Gln
CA382553620
NM_000051.4:c.6442A>C