Canonical Allele Identifier: PA2826630734
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2831521
ClinVar RCV Id: RCV003758275

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val292Asp
CA346749244
NM_001281493.2:c.875T>A