Canonical Allele Identifier: PA2826633411
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187154
ClinVar RCV Id: RCV000166850 RCV000484988 RCV000629789
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.His905Asp
CA013567
NM_001281493.2:c.2713C>G