Allele Registry

Canonical Allele Identifier: PA105999

Gene: KRT2 HGNC NCBI

ClinVar RCV:

RCV000009893

RCV000056533

ClinVar Variation:

9309

HGVS (amino-acid)	Matching Registered Transcripts
NP_000414.2:p.Glu487Asp	CA120290 NM_000423.3:c.1461G>T CA384929568 NM_000423.3:c.1461G>C