Canonical Allele Identifier: PA645414689
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 263543
ClinVar RCV Id: RCV000254469 RCV001206578 RCV001700025
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe230Ser
CA10587777
NM_000257.4:c.689T>C