Canonical Allele Identifier: PA2828108808
Gene: SLC4A11 HGNC NCBI

Linked Data

ClinVar Variation Id: 338257
ClinVar RCV Id: RCV000271561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350674.1:p.Arg137Trp
CA9742303
NM_001363745.1:c.409C>T