Canonical Allele Identifier: PA216668
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 66213
ClinVar RCV Id: RCV000056559 RCV001332429 RCV001115027 RCV001197761 RCV003989310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000415.2:p.Arg471Cys
CA216667
NM_000424.4:c.1411C>T