Canonical Allele Identifier: PA2825033040
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1442772
ClinVar RCV Id: RCV001953159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe1368Leu
CA382528619
NM_000051.4:c.4102T>C
CA382528669
NM_000051.4:c.4104T>A
CA382528673
NM_000051.4:c.4104T>G