Canonical Allele Identifier: PA658674702
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1449Phe
CA6265438
NM_000051.4:c.4347A>C
CA382531987
NM_000051.4:c.4347A>T