Canonical Allele Identifier: PA104233
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 14607
ClinVar RCV Id: RCV000015711 RCV000057025 RCV004017253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Lys354Asn
CA217370
NM_005557.4:c.1062A>T
CA399490153
NM_005557.4:c.1062A>C