Canonical Allele Identifier: PA916033809
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2955490
ClinVar RCV Id: RCV003810641
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser2057Leu
CA382550682
NM_001351834.2:c.6170C>T