Canonical Allele Identifier: PA097694
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177627
ClinVar RCV Id: RCV000663405 RCV000786922 RCV000618360 RCV000628970 RCV001723720 RCV003531980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg694Cys
CA011642
NM_000257.4:c.2080C>T