Canonical Allele Identifier: PA2825143457
Gene: SLC12A3 HGNC NCBI
ClinVar RCV:
RCV000009125
ClinVar Variation:
8594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Gly630Val
CA119778
NM_000339.3:c.1889G>T