Canonical Allele Identifier: PA174056
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 132928
ClinVar RCV Id: RCV000148977
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala423Thr
CA010450
NM_000257.4:c.1267G>A