Canonical Allele Identifier: PA2825350343
Gene: INF2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Ala28Val
CA391224777
NM_001031714.3:c.83C>T