Canonical Allele Identifier: PA2499270543
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025296
ClinVar RCV Id: RCV001325597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Thr770Ser
CA394822957
NM_005236.3:c.2308A>T
CA394822962
NM_005236.3:c.2309C>G