Canonical Allele Identifier: PA645435467
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 335664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Pro433Ser
CA1592458
NM_001029883.3:c.1297C>T