Canonical Allele Identifier: PA103893
Gene: KRT6A HGNC NCBI

Linked Data

ClinVar Variation Id: 66589
ClinVar RCV Id: RCV000057011 RCV000128821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005545.1:p.Asn171Lys
CA217356
NM_005554.4:c.513C>A
CA384963368
NM_005554.4:c.513C>G