Canonical Allele Identifier: PA891844933
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 569619
ClinVar RCV Id: RCV000690296
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala917Ile
CA891844298
NM_000257.4:c.2749_2750delinsAT