Canonical Allele Identifier: PA658817881
Gene: COL12A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 542494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004361.3:p.Met1582Leu
CA3893356
NM_004370.6:c.4744A>C
CA364742260
NM_004370.6:c.4744A>T