Canonical Allele Identifier: PA203992
Gene: COL12A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 204297
ClinVar RCV Id: RCV000186501 RCV000441199 RCV000702038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004361.3:p.Arg1965Cys
CA203991
NM_004370.6:c.5893C>T