Canonical Allele Identifier: PA111919
Gene: PRLR HGNC NCBI

Linked Data

ClinVar Variation Id: 88996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000940.1:p.Ile170Leu
CA145411
NM_000949.7:c.508A>C