Canonical Allele Identifier: PA915958917
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 14617
ClinVar RCV Id: RCV000015721 RCV000056753
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Met272Arg
CA216982
NM_000526.5:c.815T>G