Allele Registry

Canonical Allele Identifier: PA103903

Gene: KRT6A HGNC NCBI

ClinVar RCV:

RCV000057010

RCV000128820

ClinVar Variation:

66588

HGVS (amino-acid)	Matching Registered Transcripts
NP_005545.1:p.Asn171Ser	CA217355 NM_005554.4:c.512A>G