Canonical Allele Identifier: PA1139674653
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 967644
ClinVar RCV Id: RCV001242607
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1431Gly
CA041540
NM_000257.4:c.4292A>G