Allele Registry

Canonical Allele Identifier: PA206088

Gene: TYRP1 HGNC NCBI

ClinVar RCV:

RCV000192929

ClinVar Variation:

212527

HGVS (amino-acid)	Matching Registered Transcripts
NP_000541.1:p.Leu382Pro	CA206087 NM_000550.3:c.1145T>C