Canonical Allele Identifier: PA2573076367
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 66171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366295.1:p.Gly126Ser
CA216584
NM_001379366.1:c.376G>A