Canonical Allele Identifier: PA2825350745
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 472869
ClinVar RCV Id: RCV000531677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Leu185Pro
CA391213259
NM_001031714.3:c.554T>C