Canonical Allele Identifier: PA203988
Gene: COL12A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 204295
ClinVar RCV Id: RCV000186499 RCV000480507 RCV000664222 RCV000850513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004361.3:p.Ile2334Thr
CA203987
NM_004370.6:c.7001T>C