Canonical Allele Identifier: PA123074
Gene: INS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000198.1:p.Phe49Leu
CA123073
NM_000207.3:c.147C>G
CA379121476
NM_000207.3:c.147C>A
CA379121492
NM_000207.3:c.145T>C