Canonical Allele Identifier: PA2825490465
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046910
ClinVar RCV Id: RCV001351531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077071.1:p.Leu1072Val
CA374111726
NM_001083602.3:c.3214C>G