Canonical Allele Identifier: PA645502843
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233648
ClinVar RCV Id: RCV000213546 RCV000824580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro1526Ser
CA10579155
NM_000051.4:c.4576C>T