Canonical Allele Identifier: PA104151
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 14602
ClinVar RCV Id: RCV000015706 RCV000057037 RCV000144080 RCV000763397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Asn125Ser
CA124158
NM_005557.4:c.374A>G