ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916015513
Gene: SLC40A1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
698027
ClinVar RCV Id:
RCV000865209
RCV003918370
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_055400.1:p.Pro443Leu
CA2024082
NM_014585.6:c.1328C>T