Canonical Allele Identifier: PA2826629545
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 951825
ClinVar RCV Id: RCV001223820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser13Phe
CA46707062
NM_001281493.2:c.38C>T