Canonical Allele Identifier: PA891845023
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 581683
ClinVar RCV Id: RCV000705585 RCV001816734 RCV001177310
ClinVar Variation Id: 2568229
ClinVar RCV Id: RCV003283557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met855Leu
CA6265061
NM_000051.4:c.2563A>T
CA382543804
NM_000051.4:c.2563A>C