Allele Registry

Canonical Allele Identifier: PA101075

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000003996

RCV000085959

ClinVar Variation:

3793

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Pro21Ser	CA227575 NM_000372.5:c.61C>T