Canonical Allele Identifier: PA2499230336
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1031478
ClinVar RCV Id: RCV001333313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly984Val
CA389046438
NM_000257.4:c.2951G>T