Allele Registry

Canonical Allele Identifier: PA124263

Gene: INSR HGNC NCBI

Linked Data

ClinVar RCV:

RCV000015822

RCV000175131

RCV000344820

RCV000445519

RCV000515071

RCV001132183

RCV001132184

RCV001258250

ClinVar Variation:

14707

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Val1012Met	CA124262 NM_000208.4:c.3034G>A