Canonical Allele Identifier: PA916051560
Gene: HSPA12B HGNC NCBI

Linked Data

ClinVar Variation Id: 715749
ClinVar RCV Id: RCV000888263
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443202.3:p.Val23Leu
CA9747615
NM_052970.5:c.67G>C
CA408132037
NM_052970.5:c.67G>T