Canonical Allele Identifier: PA913191647
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 630066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe1336Leu
CA382527507
NM_000051.4:c.4006T>C
CA382527523
NM_000051.4:c.4008C>A
CA382527531
NM_000051.4:c.4008C>G