ClinGen Allele Registry
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Canonical Allele Identifier:
PA158929
Gene: ERCC4
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000120828
RCV000283278
RCV001521901
RCV001668273
ClinVar Variation:
134155
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005227.1:p.Arg415Gln
CA158927
NM_005236.3:c.1244G>A