Canonical Allele Identifier: PA2825035783
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2910291
ClinVar RCV Id: RCV003607088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn2603Tyr
CA382561275
NM_000051.4:c.7807A>T