Canonical Allele Identifier: PA916034471
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127448
ClinVar RCV Id: RCV000115254 RCV000205594 RCV000589821 RCV000855570 RCV003153367 RCV004549572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2580Ser
CA286994
NM_001351834.2:c.7740A>C
CA382561122
NM_001351834.2:c.7740A>T