Canonical Allele Identifier: PA916011983
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182647
ClinVar RCV Id: RCV000160695 RCV000464912 RCV000573393 RCV003998503
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val871Met
CA013259
NM_001281494.2:c.2611G>A