Canonical Allele Identifier: PA2580202451
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2087496
ClinVar RCV Id: RCV003017866
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu304Asp
CA382530487
NM_001351834.2:c.912A>C
CA382530488
NM_001351834.2:c.912A>T