Canonical Allele Identifier: PA2580113725
Gene: TYR HGNC NCBI
ClinVar RCV:
RCV003044103
ClinVar Variation:
2126395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Val25Ala
CA382033270
NM_000372.5:c.74T>C