Canonical Allele Identifier: PA2573168809
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1433302
ClinVar RCV Id: RCV001960069
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Asn86Lys
CA382033965
NM_000372.5:c.258T>G
CA382033969
NM_000372.5:c.258T>A