Canonical Allele Identifier: PA645506485
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 331823
ClinVar RCV Id: RCV000277941 RCV000330744 RCV000465241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Lys965Asn
CA1941664
NM_024753.5:c.2895A>T
CA349049785
NM_024753.5:c.2895A>C