Canonical Allele Identifier: PA645402487
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 435517
ClinVar RCV Id: RCV000503966 RCV000765477 RCV001302076 RCV003884579
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Asp1259Asn
CA9135155
NM_000208.4:c.3775G>A