Canonical Allele Identifier: PA913197147
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 617794
ClinVar RCV Id: RCV000755067 RCV000785610 RCV003558555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Cys55Ser
CA6221052
NM_000372.5:c.164G>C
CA382033599
NM_000372.5:c.163T>A