Canonical Allele Identifier: PA645492954
Gene: TINF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036593.2:p.Gln21Arg
CA7130763
NM_012461.2:c.62A>G