Canonical Allele Identifier: PA2826635464
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu339del
CA009463
NM_001281494.2:c.1015_1017del
CA346750222
NM_001281494.2:c.1009G>T
CA346750265
NM_001281494.2:c.1012G>T
CA346750292
NM_001281494.2:c.1015G>T