Canonical Allele Identifier: PA2829340203
Gene: C1S HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001725.1:p.Ala11Leu
CA2573148408
NM_001734.5:c.31_32delinsTT