Canonical Allele Identifier: PA2826173125
Gene: HSPA12B HGNC NCBI

Linked Data

ClinVar Variation Id: 715749
ClinVar RCV Id: RCV000888263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184256.1:p.Val23Leu
CA9747615
NM_001197327.2:c.67G>C
CA408132037
NM_001197327.2:c.67G>T