Canonical Allele Identifier: PA2580113727
Gene: TYR HGNC NCBI
ClinVar RCV:
RCV003062440
ClinVar Variation:
2137221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Asn29Lys
CA6221035
NM_000372.5:c.87C>A
CA382033334
NM_000372.5:c.87C>G