Canonical Allele Identifier: PA2825112152
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069380
ClinVar RCV Id: RCV004007924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1031Leu
CA389045646
NM_000257.4:c.3091G>T
CA389045647
NM_000257.4:c.3091G>C