Allele Registry

Canonical Allele Identifier: PA2573062993

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV001775534

ClinVar Variation:

1321191

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Tyr415_Glu420del	CA2573054422 NM_000526.5:c.1242_1259del