Canonical Allele Identifier: PA645498615
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232670
ClinVar RCV Id: RCV000220838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe212Leu
CA10578968
NM_000051.4:c.634T>C
CA382528412
NM_000051.4:c.636T>A
CA382528415
NM_000051.4:c.636T>G