Canonical Allele Identifier: PA185288
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 179858
ClinVar RCV Id: RCV000156658 RCV001306103
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1555Gln
CA015206
NM_000257.4:c.4663G>C