Allele Registry

Canonical Allele Identifier: PA105950

Gene: KRT2 HGNC NCBI

ClinVar RCV:

RCV000009896

ClinVar Variation:

9311

HGVS (amino-acid)	Matching Registered Transcripts
NP_000414.2:p.Gln181Pro	CA120292 NM_000423.3:c.542A>C