Canonical Allele Identifier: PA2573168779
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1379578
ClinVar RCV Id: RCV001914887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Asn62Ser
CA6221058
NM_000372.5:c.185A>G