Canonical Allele Identifier: PA645503597
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2026Ile
CA6265843
NM_000051.4:c.6078G>A
CA382550136
NM_000051.4:c.6078G>T
CA382550138
NM_000051.4:c.6078G>C