Canonical Allele Identifier: PA2825165588
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1398041
ClinVar RCV Id: RCV001912733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000412.4:p.Tyr449His
CA399390362
NM_000421.5:c.1345T>C