Canonical Allele Identifier: PA103904
Gene: KRT85 HGNC NCBI

Linked Data

ClinVar Variation Id: 6836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002274.1:p.Arg78His
CA118532
NM_002283.4:c.233G>A