Canonical Allele Identifier: PA916056893
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 93968
ClinVar RCV Id: RCV000079907 RCV000269415 RCV000329141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542197.3:p.Thr72Ser
CA221845
NM_080630.4:c.215C>G
CA341168601
NM_080630.4:c.214A>T