Canonical Allele Identifier: PA645510274
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 437986
ClinVar RCV Id: RCV000504775 RCV003464078 RCV002524403 RCV003325487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Gly346Val
CA6221333
NM_000372.5:c.1037G>T