Canonical Allele Identifier: PA916032493
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127366
ClinVar RCV Id: RCV000115171 RCV000194529 RCV000515446 RCV000588986 RCV001079613 RCV001354960 RCV002291557 RCV004549545 RCV003492454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn1005Ser
CA208751
NM_001351834.2:c.3014A>G