Canonical Allele Identifier: PA2825030885
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2580403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu419Phe
CA382533278
NM_000051.4:c.1257A>T
CA382533282
NM_000051.4:c.1257A>C