Allele Registry

Canonical Allele Identifier: PA915958900

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000015718

RCV000056739

ClinVar Variation:

14614

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Glu144Ala	CA216959 NM_000526.5:c.431A>C