Canonical Allele Identifier: PA2573163715
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501691
ClinVar RCV Id: RCV002010774 RCV003170536
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys813Asn
CA346754046
NM_000179.3:c.2439G>C
CA346754047
NM_000179.3:c.2439G>T