Canonical Allele Identifier: PA915958866
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66349
ClinVar RCV Id: RCV000056720
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Arg125Leu
CA216925
NM_000526.5:c.374G>T