Canonical Allele Identifier: PA158766
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134099
ClinVar RCV Id: RCV000120771 RCV000662069 RCV000662070 RCV000662071 RCV000764209 RCV001329853 RCV001854613 RCV002256052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000391.1:p.Gln629His
CA158764
NM_000400.4:c.1887G>C
CA406363733
NM_000400.4:c.1887G>T