Allele Registry

Canonical Allele Identifier: PA216636

Gene: KRT2 HGNC NCBI

ClinVar RCV:

RCV000056536

ClinVar Variation:

66194

HGVS (amino-acid)	Matching Registered Transcripts
NP_000414.2:p.Gln181Leu	CA216635 NM_000423.3:c.542A>T