Canonical Allele Identifier: PA2826630979
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 820355
ClinVar RCV Id: RCV001013728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile349Leu
CA346750538
NM_001281493.2:c.1045A>C