Canonical Allele Identifier: PA2825352171
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 432619
ClinVar RCV Id: RCV000497978 RCV003766802
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Ala1165Val
CA7373277
NM_001031714.3:c.3494C>T