Canonical Allele Identifier: PA2741880329
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2554203
ClinVar RCV Id: RCV003304137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366295.1:p.Ser13Phe
CA399396747
NM_001379366.1:c.38C>T