Canonical Allele Identifier: PA658813644
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 528908
ClinVar RCV Id: RCV000634203 RCV001496568 RCV004544823 RCV002279455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Gly171Arg
CA1942419
NM_024753.5:c.511G>A
CA349051976
NM_024753.5:c.511G>C