Canonical Allele Identifier: PA2825165533
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1600017
ClinVar RCV Id: RCV002117882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000412.4:p.Ile101Ser
CA8548324
NM_000421.5:c.302T>G