Allele Registry

Canonical Allele Identifier: PA2829180399

Gene: KRT40 HGNC NCBI

ClinVar Allele:

2236627

ClinVar RCV:

RCV004110602

ClinVar Variation:

2255854

HGVS (amino-acid)	Matching Registered Transcripts
NP_001376173.1:p.Arg362His	CA8550311 NM_001389244.1:c.1085G>A