Allele Registry

Canonical Allele Identifier: PA2741816403

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV003740029

ClinVar Variation:

2915508

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Arg416Cys	CA8562466 NM_000526.5:c.1246C>T