Canonical Allele Identifier: PA2826016491
Gene: ERCC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159521.1:p.Phe231Leu
CA126880
NM_001166049.2:c.693C>G
CA406355844
NM_001166049.2:c.693C>A
CA406355851
NM_001166049.2:c.691T>C