Canonical Allele Identifier: PA2828102077
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_001350597.1:p.Pro248Ser
CA343180
NM_001363668.2:c.742C>T