ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645482005
Gene: F13B
HGNC
NCBI
Linked Data
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Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_001985.2:p.Ser654Phe
NM_001994.3:c.1961C>T