Canonical Allele Identifier: PA645483964
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 309568
ClinVar RCV Id: RCV000278442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000415.2:p.Phe127Leu
CA10633194
NM_000424.4:c.381C>A
CA384929534
NM_000424.4:c.381C>G
CA384929542
NM_000424.4:c.379T>C