Canonical Allele Identifier: PA645383057
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 433918
ClinVar RCV Id: RCV000499422 RCV000573654 RCV003470622 RCV001350778
ClinVar Variation Id: 1511890
ClinVar RCV Id: RCV002020639 RCV002441213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu983Asp
CA069854
NM_000179.3:c.2949G>C
CA346756238
NM_000179.3:c.2949G>T