Canonical Allele Identifier: PA645419870
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 418532
ClinVar RCV Id: RCV000789027 RCV001109651 RCV000486643 RCV000765023 RCV003488627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Asp305Glu
CA6221261
NM_000372.5:c.915C>A
CA382035868
NM_000372.5:c.915C>G