Canonical Allele Identifier: PA658679951
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483882
ClinVar RCV Id: RCV000575336 RCV000824221 RCV004001066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro15Ala
CA346734536
NM_000179.3:c.43C>G