Canonical Allele Identifier: PA2829948501
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005347
ClinVar RCV Id: RCV001302204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065759.1:p.Met1035Ile
CA9887782
NM_020708.5:c.3105G>A
CA409208323
NM_020708.5:c.3105G>C
CA409208325
NM_020708.5:c.3105G>T