Canonical Allele Identifier: PA216660
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 66208
ClinVar RCV Id: RCV000056554 RCV001352785
ClinVar Variation Id: 2765862
ClinVar RCV Id: RCV003578525 RCV003985905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000415.2:p.Glu466Asp
CA216659
NM_000424.4:c.1398G>C
CA384923569
NM_000424.4:c.1398G>T