Canonical Allele Identifier: PA916032101
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 639227
ClinVar RCV Id: RCV000791970 RCV001014845
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr741Ser
CA382539127
NM_001351834.2:c.2222A>C