Canonical Allele Identifier: PA645468854
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 309610
ClinVar RCV Id: RCV000403358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Glu351Lys
CA6585621
NM_000423.3:c.1051G>A