Canonical Allele Identifier: PA2580234829
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1965147
ClinVar RCV Id: RCV002726586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366295.1:p.Phe67Leu
CA399396299
NM_001379366.1:c.201T>G
CA399396301
NM_001379366.1:c.201T>A
CA399396310
NM_001379366.1:c.199T>C