Canonical Allele Identifier: PA2825034551
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2955490
ClinVar RCV Id: RCV003810641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2057Leu
CA382550682
NM_000051.4:c.6170C>T