Canonical Allele Identifier: PA916034377
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478949
ClinVar RCV Id: RCV000574835 RCV000764946 RCV001217033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met2503Leu
CA6266118
NM_001351834.2:c.7507A>T
CA382560592
NM_001351834.2:c.7507A>C