Canonical Allele Identifier: PA658801679
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524368
ClinVar RCV Id: RCV000628102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1836Val
CA382545701
NM_000051.4:c.5507A>T