Canonical Allele Identifier: PA658670898
Gene: COL12A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 452137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004361.3:p.His1256Leu
CA3893627
NM_004370.6:c.3767A>T