Canonical Allele Identifier: PA104193
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 66606
ClinVar RCV Id: RCV000057033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Leu124Pro
CA217380
NM_005557.4:c.371T>C