Canonical Allele Identifier: PA916033570
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 426534
ClinVar RCV Id: RCV000489997 RCV000546553 RCV000569421 RCV000780900 RCV003316640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1878Leu
CA6265741
NM_001351834.2:c.5633C>T