Canonical Allele Identifier: PA645483870
Gene: KRT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 432177
ClinVar RCV Id: RCV000497739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006112.3:p.Ala450Asp
CA384962844
NM_006121.4:c.1349C>A