Canonical Allele Identifier: PA916010916
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483882
ClinVar RCV Id: RCV000575336 RCV000824221 RCV004001066
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro15Ala
CA346734536
NM_001281492.2:c.43C>G