Canonical Allele Identifier: PA645483974
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 379242
ClinVar RCV Id: RCV000435783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000415.2:p.Asp158Tyr
CA16606334
NM_000424.4:c.472G>T