Allele Registry

Canonical Allele Identifier: PA2573062990

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV001823427

ClinVar Variation:

1338973

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Arg125Ser	CA399482518 NM_000526.5:c.373C>A