Canonical Allele Identifier: PA916034522
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 574618
ClinVar RCV Id: RCV000696595 RCV001026894 RCV001798962 RCV003480779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys2624Ser
CA6266205
NM_001351834.2:c.7871G>C
CA382561411
NM_001351834.2:c.7870T>A