Canonical Allele Identifier: PA176974
Gene: MYH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 164257
ClinVar RCV Id: RCV000208506 RCV000151226 RCV000995139 RCV002390325 RCV002498699 RCV001321909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002462.2:p.Arg54Gln
CA176972
NM_002471.4:c.161G>A