Canonical Allele Identifier: PA102212
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 56002
ClinVar RCV Id: RCV000049411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Met136Ile
CA144102
NM_000111.3:c.408G>A
CA368853745
NM_000111.3:c.408G>T
CA368853746
NM_000111.3:c.408G>C