Canonical Allele Identifier: PA658670580
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453709
ClinVar RCV Id: RCV000562052 RCV000550643 RCV001030603 RCV003470687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2635Gly
CA382561483
NM_000051.4:c.7904C>G