Canonical Allele Identifier: PA158920
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 134152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Pro472Leu
CA158918
NM_005236.3:c.1415C>T