Canonical Allele Identifier: PA645501628
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407683
ClinVar RCV Id: RCV000470743 RCV000575167 RCV000481741 RCV001358722 RCV003470439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1080Glu
CA6265231
NM_000051.4:c.3240C>A
CA382515985
NM_000051.4:c.3240C>G