Allele Registry

Canonical Allele Identifier: PA2741816391

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV003728869

ClinVar Variation:

2899219

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Ala157Ser	CA399481982 NM_000526.5:c.469G>T CA2739267535 NM_000526.5:c.468_470delinsCAG