Allele Registry

Canonical Allele Identifier: PA103882

Gene: KRT6A HGNC NCBI

ClinVar Allele:

77482

ClinVar RCV:

RCV000057007

RCV000128818

ClinVar Variation:

66585

HGVS (amino-acid)	Matching Registered Transcripts
NP_005545.1:p.Asn171Asp	CA217351 NM_005554.4:c.511A>G