Canonical Allele Identifier: PA2825112112
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2757321
ClinVar RCV Id: RCV003587809
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala990Pro
CA389046384
NM_000257.4:c.2968G>C
CA2697553843
NM_000257.4:c.2967_2968delinsCC