Canonical Allele Identifier: PA277513
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 216955
ClinVar RCV Id: RCV000198279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Gln122Arg
CA277512
NM_005557.4:c.365A>G