Canonical Allele Identifier: PA645503112
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407496
ClinVar RCV Id: RCV000463817 RCV000580727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg1730Leu
CA16613065
NM_000051.4:c.5189G>T