Canonical Allele Identifier: PA100328
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 99528
ClinVar RCV Id: RCV000085890 RCV001588915 RCV003460774 RCV004529898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Ala355Pro
CA227490
NM_000372.5:c.1063G>C