Canonical Allele Identifier: PA645506454
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 281236
ClinVar RCV Id: RCV000360722 RCV001134207 RCV001134208 RCV001859543 RCV002487181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Met844Val
CA1941809
NM_024753.5:c.2530A>G