Canonical Allele Identifier: PA2499271261
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 1049150
ClinVar RCV Id: RCV001354876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Gly59Trp
CA399496066
NM_005557.4:c.175G>T