ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA122628
Gene: TSHB
HGNC
NCBI
Linked Data
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Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_000540.2:p.Gly49Arg
NM_000549.5:c.145G>A
NM_000549.5:c.145G>C