Canonical Allele Identifier: PA2826271038
Gene: PRLR HGNC NCBI

Linked Data

ClinVar Variation Id: 88996
ClinVar RCV Id: RCV000074480 RCV003974953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191246.1:p.Ile170Leu
CA145411
NM_001204317.1:c.508A>C