Canonical Allele Identifier: PA217337
Gene: KRT6A HGNC NCBI

Linked Data

ClinVar Variation Id: 66573
ClinVar RCV Id: RCV000056993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005545.1:p.Tyr465Cys
CA217336
NM_005554.4:c.1394A>G