Canonical Allele Identifier: PA645506371
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 261785
ClinVar RCV Id: RCV000250774 RCV001570982 RCV001854968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Asn320Lys
CA1942274
NM_024753.5:c.960C>G
CA349066872
NM_024753.5:c.960C>A