Canonical Allele Identifier: PA124276
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14714
ClinVar RCV Id: RCV000015829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Asn458Asp
CA124275
NM_001079817.3:c.1372A>G