Allele Registry

Canonical Allele Identifier: PA915958859

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000015733

RCV000056713

RCV003690945

ClinVar Variation:

14628

2851007

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Asn123Ser	CA216911 NM_000526.5:c.368A>G CA2739267536 NM_000526.5:c.368_369delinsGC