Canonical Allele Identifier: PA645415085
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 282910
ClinVar RCV Id: RCV000259647 RCV000299908 RCV000354703 RCV000367416 RCV000361664 RCV000407213 RCV001084518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Met504Ile
CA3505452
NM_000112.4:c.1512G>A
CA129084421
NM_000112.4:c.1512G>T
CA361708018
NM_000112.4:c.1512G>C