Canonical Allele Identifier: PA2741863677
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2835245
ClinVar RCV Id: RCV003606528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Gln51del
CA2739270897
NM_001351836.2:c.151_153del