Canonical Allele Identifier: PA2828329803
Gene: ERCC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356345.1:p.Phe231Leu
CA126880
NM_001369416.1:c.693C>G
CA406355844
NM_001369416.1:c.693C>A
CA406355851
NM_001369416.1:c.691T>C