Allele Registry

Canonical Allele Identifier: PA915958855

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056711

ClinVar Variation:

66343

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Gln120Arg	CA216907 NM_000526.5:c.359A>G