Canonical Allele Identifier: PA2825504023
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 646094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Ser981Phe
CA374111756
NM_001083604.3:c.2942C>T