Canonical Allele Identifier: PA2826626497
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234483
ClinVar RCV Id: RCV000215890 RCV000225881 RCV000662360 RCV000569553 RCV004541361 RCV003998620
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly490Ser
CA10577265
NM_001281492.2:c.1468G>A