Canonical Allele Identifier: PA2825448014
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2663319
ClinVar RCV Id: RCV003442507
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Gly1020Ser
CA403671323
NM_001079817.3:c.3058G>A