Canonical Allele Identifier: PA2825165542
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 66171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000412.4:p.Gly126Ser
CA216584
NM_000421.5:c.376G>A