Canonical Allele Identifier: PA2825165538
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2270826
ClinVar RCV Id: RCV002809760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000412.4:p.Gly108Arg
CA8548318
NM_000421.5:c.322G>A
CA399395619
NM_000421.5:c.322G>C