Canonical Allele Identifier: PA2826666465
Gene: KCTD17 HGNC NCBI

Linked Data

ClinVar Variation Id: 476040
ClinVar RCV Id: RCV000548348 RCV001722521 RCV003980035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269615.2:p.Arg212Trp
CA10215202
NM_001282686.2:c.634C>T