Canonical Allele Identifier: PA100819
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 99562
ClinVar RCV Id: RCV000085945 RCV000626679 RCV003460780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Gly109Arg
CA227559
NM_000372.5:c.325G>A
CA382034155
NM_000372.5:c.325G>C