Canonical Allele Identifier: PA2826568200
Gene: ERCC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 300092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263987.1:p.Lys286Asn
CA5496425
NM_001277058.2:c.858G>C
CA376754328
NM_001277058.2:c.858G>T