Canonical Allele Identifier: PA2826631157
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676789
ClinVar RCV Id: RCV003470245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Phe387Leu
CA346750785
NM_001281493.2:c.1159T>C
CA346750790
NM_001281493.2:c.1161C>A
CA346750791
NM_001281493.2:c.1161C>G