Canonical Allele Identifier: PA215389
Gene: PDLIM3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055291.2:p.Val127Met
CA215388
NM_014476.6:c.379G>A