Allele Registry

Canonical Allele Identifier: PA2741816390

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV003729099

ClinVar Variation:

2904064

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Arg155Trp	CA8562715 NM_000526.5:c.463C>T