Canonical Allele Identifier: PA2741867652
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2807738
ClinVar RCV Id: RCV003606115
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2626Gly
CA382561426
NM_001351834.2:c.7877C>G