Canonical Allele Identifier: PA298184
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181934
ClinVar RCV Id: RCV000159700 RCV000456359 RCV000565271 RCV001251294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu885Phe
CA298182
NM_000051.4:c.2655A>T
CA382545041
NM_000051.4:c.2655A>C