Canonical Allele Identifier: PA1139671761
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 928851
ClinVar RCV Id: RCV001193367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly231Val
CA389052246
NM_000257.4:c.692G>T