Linked Data
dbSNP Id:
rs2740980
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12312201G>C , CM000686.2:g.12312201G>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000651802.1:n.451-70793C>G | ||
| ENST00000651835.1:n.320-54170C>G |