Canonical Allele Identifier: PA2825350544
Gene: INF2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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