Canonical Allele Identifier: PA2580276079
Gene: KRT81 HGNC NCBI

Linked Data

ClinVar Variation Id: 2287118
ClinVar RCV Id: RCV004139121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002272.2:p.Ser491Arg
CA384913323
NM_002281.4:c.1473C>G
CA384913324
NM_002281.4:c.1473C>A
CA384913329
NM_002281.4:c.1471A>C