Canonical Allele Identifier: PA2825030901
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 818770
ClinVar RCV Id: RCV001010692 RCV003500616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala425Val
CA382533440
NM_000051.4:c.1274C>T