Canonical Allele Identifier: PA198945
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1478511
ClinVar RCV Id: RCV001998634
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu277Val
CA016861
NM_000257.4:c.829C>G