Canonical Allele Identifier: PA2499256466
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1030782
ClinVar RCV Id: RCV001332428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366295.1:p.Ser33Phe
CA8548360
NM_001379366.1:c.98C>T