Canonical Allele Identifier: PA2741867157
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2682297
ClinVar RCV Id: RCV003479670 RCV003500863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe1870Leu
CA382546271
NM_001351834.2:c.5608T>C
CA382546283
NM_001351834.2:c.5610C>A
CA382546285
NM_001351834.2:c.5610C>G