Canonical Allele Identifier: PA2825351061
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312684
ClinVar RCV Id: RCV000393663 RCV002446566 RCV002480127
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Thr376Ser
CA10639830
NM_001031714.3:c.1126A>T
CA391215914
NM_001031714.3:c.1127C>G