Allele Registry

Canonical Allele Identifier: PA645468825

Gene: KRT2 HGNC NCBI

ClinVar RCV:

RCV000370371

RCV000434387

ClinVar Variation:

309618

HGVS (amino-acid)	Matching Registered Transcripts
NP_000414.2:p.Arg179His	CA6585819 NM_000423.3:c.536G>A