Canonical Allele Identifier: PA2499230277
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1008293
ClinVar RCV Id: RCV001305598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1434Gly
CA389040172
NM_000257.4:c.4300C>G