Canonical Allele Identifier: PA2827629848
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187213
ClinVar Variation Id: 3148226
ClinVar RCV Id: RCV004440130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338764.1:p.Met1Leu