Canonical Allele Identifier: PA2573163684
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1428818
ClinVar RCV Id: RCV001936488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp797Asn
CA346753817
NM_000179.3:c.2389G>A