Canonical Allele Identifier: PA915958879
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66357
ClinVar RCV Id: RCV000056728
ClinVar Variation Id: 66358
ClinVar RCV Id: RCV000056729 RCV001352828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Val133Leu
CA216939
NM_000526.5:c.397G>C
CA216941
NM_000526.5:c.397G>T