Canonical Allele Identifier: PA106473
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 14648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000415.2:p.Pro25Leu
CA216792
NM_000424.4:c.74C>T