Canonical Allele Identifier: PA270041
Gene: PRCD HGNC NCBI

Linked Data

ClinVar Variation Id: 143095
ClinVar RCV Id: RCV000132616 RCV000678599 RCV001060810 RCV003888552
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071088.1:p.Met1Thr