Canonical Allele Identifier: PA2825034521
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 664216
ClinVar RCV Id: RCV000822260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2046Val
CA382550507
NM_000051.4:c.6136C>G