ClinGen Allele Registry
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Canonical Allele Identifier:
PA915973383
Gene: ERCC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
16784
ClinVar RCV Id:
RCV000018274
RCV000018273
RCV000424822
RCV003466865
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001124339.1:p.Arg88His
CA126883
NM_001130867.2:c.263G>A