Canonical Allele Identifier: PA2825447825
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2627655
ClinVar RCV Id: RCV004362766
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Ala550Val
CA403666642
NM_001079817.3:c.1649C>T