Canonical Allele Identifier: PA916033461
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524272
ClinVar RCV Id: RCV000627921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys1782Asn
CA382543196
NM_001351834.2:c.5346A>C
CA382543199
NM_001351834.2:c.5346A>T