Allele Registry

Canonical Allele Identifier: PA2573170995

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV002249092

ClinVar Variation:

1685365

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Met119Arg	CA399482585 NM_000526.5:c.356T>G