Canonical Allele Identifier: PA645294276
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 265217
ClinVar RCV Id: RCV000255715 RCV002494798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Arg127Gly
CA10588649
NM_005557.4:c.379C>G