Canonical Allele Identifier: PA104261
Gene: OCA2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000266.2:p.Met394Ile
CA251641
NM_000275.3:c.1182G>A
CA391361793
NM_000275.3:c.1182G>T
CA391361794
NM_000275.3:c.1182G>C