Canonical Allele Identifier: PA645401918
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 317816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Arg576Ser
CA7910523
NM_005236.3:c.1728A>T
CA394812523
NM_005236.3:c.1728A>C