Canonical Allele Identifier: PA177009
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164305
ClinVar RCV Id: RCV000151251 RCV000766443
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1079Gly
CA013459
NM_000257.4:c.3235C>G