Canonical Allele Identifier: PA658673876
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481260
ClinVar RCV Id: RCV000564336 RCV000628031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met660Thr
CA382536867
NM_000051.4:c.1979T>C