Canonical Allele Identifier: PA2826155700
Gene: INS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172027.1:p.Phe49Leu
CA123073
NM_001185098.2:c.147C>G
CA379121476
NM_001185098.2:c.147C>A
CA379121492
NM_001185098.2:c.145T>C