Canonical Allele Identifier: PA103903
Gene: KRT6A HGNC NCBI

Linked Data

ClinVar Variation Id: 66588
ClinVar RCV Id: RCV000057010 RCV000128820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005545.1:p.Asn171Ser
CA217355
NM_005554.4:c.512A>G