Canonical Allele Identifier: PA217341
Gene: KRT6A HGNC NCBI

Linked Data

ClinVar Variation Id: 66577
ClinVar RCV Id: RCV000056999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005545.1:p.Glu472Asp
CA217340
NM_005554.4:c.1416G>C
CA384953276
NM_005554.4:c.1416G>T