Canonical Allele Identifier: PA645468803
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 309627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Arg45His
CA6585960
NM_000423.3:c.134G>A