Canonical Allele Identifier: PA1139749556
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 969327
ClinVar RCV Id: RCV001244649 RCV004034800
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Met1305Ile
CA376830326
NM_032578.4:c.3915G>A
CA376830327
NM_032578.4:c.3915G>C
CA376830328
NM_032578.4:c.3915G>T