Canonical Allele Identifier: PA343181
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38920
ClinVar RCV Id: RCV000032171 RCV000428138 RCV003407386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092744.1:p.Pro283Ser
CA343180
NM_001099274.3:c.847C>T