Canonical Allele Identifier: PA916011409
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525751
ClinVar RCV Id: RCV000630015 RCV000771661 RCV003332215 RCV004002789
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro956Ser
CA346758131
NM_001281492.2:c.2866C>T