Canonical Allele Identifier: PA645475891
Gene: INA HGNC NCBI

Linked Data

ClinVar Variation Id: 402160
ClinVar RCV Id: RCV000454151
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116116.1:p.Gly188Arg
CA16609522
NM_032727.3:c.562G>A
CA377972207
NM_032727.3:c.562G>C