Canonical Allele Identifier: PA229228
Gene: KRT39 HGNC NCBI

Linked Data

ClinVar Variation Id: 100899
ClinVar RCV Id: RCV000087261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_998821.3:p.Arg487Ser
CA229227
NM_213656.4:c.1461A>C
CA399397220
NM_213656.4:c.1461A>T