Canonical Allele Identifier: PA2825350544
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 472835
ClinVar RCV Id: RCV001378572
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Val105Glu
CA391225858
NM_001031714.3:c.314T>A