Canonical Allele Identifier: PA164914
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141251
ClinVar RCV Id: RCV000129681 RCV000590311 RCV001079129 RCV001356176 RCV001731482 RCV003149894 RCV004551246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val630Met
CA164912
NM_000051.4:c.1888G>A