Canonical Allele Identifier: PA1139671140
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 856816
ClinVar RCV Id: RCV001062363
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu5Asp
CA389054220
NM_000257.4:c.15G>T
CA389054221
NM_000257.4:c.15G>C