Canonical Allele Identifier: PA2825035137
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3222662
ClinVar RCV Id: RCV004516046
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2308Asp
CA382557100
NM_000051.4:c.6923C>A