Allele Registry

Canonical Allele Identifier: PA105980

Gene: KRT2 HGNC NCBI

ClinVar RCV:

RCV000009899

RCV000056527

ClinVar Variation:

9314

HGVS (amino-acid)	Matching Registered Transcripts
NP_000414.2:p.Glu476Lys	CA120295 NM_000423.3:c.1426G>A