Canonical Allele Identifier: PA2826630291
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89195
ClinVar RCV Id: RCV000115374 RCV000212649 RCV000587662 RCV000524111 RCV001353728 RCV003997066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met190Val
CA008673
NM_001281493.2:c.568A>G