Canonical Allele Identifier: PA169091
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142675
ClinVar RCV Id: RCV000132028 RCV000410426 RCV000464603 RCV000480539 RCV003153428 RCV003462027 RCV003998130
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg243Cys
CA016337
NM_000179.3:c.727C>T