Canonical Allele Identifier: PA2741921703
Gene: KRT6B HGNC NCBI

Linked Data

ClinVar Variation Id: 2616372
ClinVar RCV Id: RCV003371655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005546.2:p.Ala175Thr
CA6580817
NM_005555.4:c.523G>A