Canonical Allele Identifier: PA916028870
Gene: ERCC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 210955
ClinVar Variation Id: 522698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333369.1:p.Trp851Arg
CA277416
NM_001346440.2:c.2551T>C
CA376721328
NM_001346440.2:c.2551T>A