Canonical Allele Identifier: PA2573204184
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1497430
ClinVar RCV Id: RCV002019829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2637His
CA382561497
NM_001351834.2:c.7911G>C
CA382561498
NM_001351834.2:c.7911G>T