Canonical Allele Identifier: PA891845328
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 574340
ClinVar RCV Id: RCV000696256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2224Leu
CA382554863
NM_000051.4:c.6670A>C
CA382554864
NM_000051.4:c.6670A>T