Canonical Allele Identifier: PA2828102095
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713990
ClinVar RCV Id: RCV002296973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350597.1:p.Lys267Asn
CA389224890
NM_001363668.2:c.801G>T
CA389224895
NM_001363668.2:c.801G>C