Canonical Allele Identifier: PA891844979
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 567807
ClinVar RCV Id: RCV000687985 RCV001293065 RCV001525309 RCV004026283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1608Cys
CA043961
NM_000257.4:c.4822C>T