Canonical Allele Identifier: PA2573168795
Gene: TYR HGNC NCBI
ClinVar RCV:
RCV001982559
ClinVar Variation:
1444715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Ser79Trp
CA382033858
NM_000372.5:c.236C>G