Canonical Allele Identifier: PA098286
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 492982
ClinVar RCV Id: RCV000584763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly1057Asp
CA389045319
NM_000257.4:c.3170G>A